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Dichloromethane → (3S)-piperidine-3-carboxylic acid hydrochloride

HRID 656335
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HRID 656335 반응식
C(OC([N:8]1[CH2:13][CH2:12][CH2:11][C@H:10]([C:14]([OH:16])=[O:15])[CH2:9]1)=O)(C)(C)C.C(Cl)[Cl:18]>Cl.O1CCOCC1>[ClH:18].[NH:8]1[CH2:13][CH2:12][CH2:11][C@H:10]([C:14]([OH:16])=[O:15])[CH2:9]1
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참가 물질

5

반응물 2

HCID 6344DichloromethaneHCID 6951168(3S)-1-((tert-butoxy)carbonyl)piperidine-3-carboxylic acid

생성물 1

HCID 24820453(3S)-piperidine-3-carboxylic acid hydrochloride

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 312751,4-Dioxane용매

실험 절차

A mixture of (3S)-1-(tert-butoxycarbonyl)piperidine-3-carboxylic acid (4.0 g, 0.017 mol) in methylene chloride (10 mL, 0.2 mol) and 4.0 M of hydrogen chloride in 1,4-dioxane (30 mL) was stirred at rt for 2 hours. The volatiles were removed in vacuo to afford the desired product in quantitative yield. The crude product was used in the following step without further purification. LCMS: m/z 166.2 (M+H)+.

후처리

  1. customThe volatiles were removed in vacuo

출처 및 근거

ORD 기록
ord-08d1610d100f426a97702e12944ff41e
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08071624B2

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