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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trifluoroacetic acid → (R)-3-amino-2-methyl-propionitrile trifluoroacetate

HRID 246127
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HRID 246127 반응식
C(OC(=O)[NH:7][CH2:8][C@H:9]([C:11]#[N:12])[CH3:10])(C)(C)C.[F:14][C:15]([F:20])([F:19])[C:16]([OH:18])=[O:17]>ClCCl>[F:14][C:15]([F:20])([F:19])[C:16]([OH:18])=[O:17].[NH2:12][CH2:11][C@@H:9]([CH3:10])[C:8]#[N:7]
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참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 86677951((R)-2-cyano-2-methylethyl)-carbamic acid tert-butyl ester

생성물 1

HCID 86677952(R)-3-amino-2-methyl-propionitrile trifluoroacetate

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

((R)-2-Cyano-2-methyl-ethyl)-carbamic acid tert-butyl ester (42 mg, 0.23 mmol) was dissolved in dichloromethane (1.2 ml) and cooled in an ice bath. Trifluoroacetic acid (0.7 ml) was slowly added and the reaction was stirred at room temperature for 3 h then evaporated and dried under high vacuum to afford (R)-3-amino-2-methyl-propionitrile trifluoroacetate which was used without further purification.

후처리

  1. temperaturecooled in an ice bath
  2. customthen evaporated
  3. customdried under high vacuum

출처 및 근거

ORD 기록
ord-18b095b4312b412a98cb285f2a192129
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08658646B2

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