United States v. Venteria Leanet Reason

Court of Appeals for the Eleventh Circuit·Decided January 12, 2018·No. 17-11134·Unpublished

Opinion

[DO NOT PUBLISH]

IN THE UNITED STATES COURT OF APPEALS

FOR THE ELEVENTH CIRCUIT

No. 17-11134

Non-Argument Calendar

D.C. Docket No. 2:16-cr-14002-RLR-3

UNITED STATES OF AMERICA, Plaintiff–Appellee,

versus

VENTERIA LEANET REASON, Defendant–Appellant.

Appeal from the United States District Court for the Southern District of Florida

(January 12, 2018)

Before TJOFLAT, JULIE CARNES, and HULL, Circuit Judges. PER CURIAM:

Venteria Leanet Reason appeals her 135-month sentence, imposed after her guilty plea, for conspiracy to import dibutylone HCI (“dibutylone”) into the United States, in violation of 21 U.S.C. §§ 952(a) and 963. Reason’s sentence is 100 months below the lower end of the Sentencing Guidelines range. 1 She argues that: (1) the District Court procedurally erred by misapplying U.S.S.G. § 2D1.1 cmt. n.6 (“Application Note 6”) and clearly erred by finding that, for purposes of calculating her offense level, MDMA and MDEA were the substances “most clearly related” to dibutylone and ethylone, respectively2; (2) the District Court erred in applying a three-point enhancement, pursuant to U.S.S.G. § 3B1.1(b), based on its finding that she was a manager or supervisor of the conspiracy; and that (3) her sentence is otherwise procedurally and substantively unreasonable because the District Court relied on a clearly erroneous fact—that a “support network” would care for her children while she was incarcerated—and because the Court failed to consider all of her arguments for a downward variance. We disagree with each of Reason’s arguments and affirm the District Court’s sentence.

1 Based on a total offense level of 38 and a criminal history category of I, Reason’s guidelines range would have been 253 to 293 months. Statutorily, however, she was subject to a maximum penalty of 240 months. Her applicable guidelines range was therefore 235 to 240 months’ imprisonment.

2 Reason’s total offense level reflects that she was held responsible for, among other substances, 10.34 kg of dibutylone and 9.98 kg of ethylone.

I.

We first address Reason’s arguments that the District Court procedurally erred by misapplying Application Note 6 and that it clearly erred by concluding that dibutylone and ethylone were most closely related to MDMA and MDEA.

We review de novo both a district court’s interpretation of the guidelines and its application of the guidelines to the facts. United States v. Barrington, 648 F.3d 1178, 1194–95 (11th Cir. 2011). Our review, further, gives due regard to the sentencing court’s opportunity to judge the credibility of witnesses. United States v. Jenkins, 901 F.2d 1075, 1083 (11th Cir. 1990).

Ethylone and dibutylone are not included in the guidelines’ Drug Quantity Table. See U.S.S.G. § 2D1.1(c). To determine the base offense level of a substance not specifically referenced in the guidelines, a court must identify the substance included in the guidelines that is “most closely related” to the unlisted substance. U.S.S.G. § 2D1.1 cmt. n.6. Then, using the most closely related substance’s marijuana-equivalency ratio as set forth in the guidelines’ Drug Equivalency Tables, the court converts the quantity of the unlisted substance to its marijuana equivalent. U.S.S.G. § 2D1.1 cmt. n.8(A), (D). To determine the most closely related substance, the court “shall, to the extent practicable, consider” three factors:

(A) Whether the controlled substance not referenced in this guideline has a chemical structure that is substantially similar to a controlled substance referenced in this guideline.

(B) Whether the controlled substance not referenced in this guideline has a stimulant, depressant, or hallucinogenic effect on the central nervous system that is substantially similar to the stimulant, depressant, or hallucinogenic effect on the central nervous system of a controlled substance referenced in this guideline.

(C) Whether a lesser or greater quantity of the controlled substance not referenced in this guideline is needed to produce a substantially similar effect on the central nervous system as a controlled substance referenced in this guideline.

U.S.S.G. § 2D1.1 cmt. n.6. The guidelines provide that one gram of either MDMA or MDEA is equivalent to 500 grams of marijuana. U.S.S.G. § 2D1.1 cmt. n.8(D). They also provide that one gram of methcathinone, the comparator substance urged by Reason, is equivalent to 380 grams of marijuana. Id.

Reason argues that the District Court procedurally erred in two ways when determining that dibutylone was most closely related to MDMA and ethylone to MDEA. First, she contends that because dibutylone and ethylone were discussed mainly as “stimulants” throughout her sentencing, while the guidelines’ Drug Equivalency Tables classify MDMA and MDEA as “hallucinogens,” see id., the Court erred in its “most closely related” determination.3 That is, if the evidence indicates that the substance at issue has one classification, the court cannot find that a substance with a different classification in the Drug Equivalency Tables is

3 The Government’s experts, though repeatedly noting the stimulant effects of dibutylone and ethylone, did not necessarily classify them as “stimulants.”

the most closely related. Second, Reason argues that the District Court misapplied the guidelines’ three-factor test outlined above.

Reason’s first argument is unpersuasive. The relevant guidelines provision instructs a court to find the substance most closely related to an unlisted substance by considering, “to the extent practicable,” similarities in the substances’ structures, effects, and potencies. U.S.S.G. § 2D1.1 cmt. n.6. There is no further requirement in the text that the comparator substance be within the same Drug Equivalency Tables classification as the unlisted substance. A number of reasons guide against reading such a requirement into the provision.

Nothing in Drug Equivalency Tables suggests its classification of substances has any bearing on a court’s “most closely related” determination. Rather, the tables assist the court in its second step: converting the unlisted substance to its marijuana equivalent after identifying the most closely related comparator. And further, the guidelines do not instruct courts to classify an unlisted substance under one of the Drug Equivalency Tables classifications in the first instance. Making courts pick a comparator substance in the same class would, without any textual support, require courts to classify the unlisted substance, as such would be necessary in order to find a comparator in the same class. What’s more, even if a court went ahead and classified the unlisted substance, there may be situations in which the substance “most closely related” to the unlisted substance under the

guidelines’ three-factor test is not within the same class. A drug with a predominantly stimulant effect might be most similar in structure and effect to a drug pegged as a hallucinogen, more so than any substance classified as a stimulant. Indeed, as the Government’s experts testified to in this case, substances can have multiple effects on a user—MDMA and MDEA have not only a hallucinogenic effect but also a strong stimulant effect, similar to that of dibutylone and ethylone. Thus, in some circumstances, Reason’s proffered requirement could negate the guidelines’ three-factor test—a court might be unable to pick the most closely related comparator under the test because the Drug Equivalency Tables classify it differently. By implication Reason therefore asks, in this situation, that we favor a textually nonexistent “requirement” over an expressly set out test. Her first argument fails.

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