홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Acetyl chloride → (1S,3S)-methyl 3-aminocyclopentanecarboxylate hydrochloride

HRID 905972
노트
인쇄 미리보기

반응식

HRID 905972 반응식
C([Cl:4])(=O)C.[CH3:5][O:6][C:7]([C@H:9]1[CH2:13][CH2:12][C@H:11]([NH:14]C(OC(C)(C)C)=O)[CH2:10]1)=[O:8]>CO>[ClH:4].[CH3:5][O:6][C:7]([C@H:9]1[CH2:13][CH2:12][C@H:11]([NH2:14])[CH2:10]1)=[O:8]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6367Acetyl chlorideHCID 2734531ST50825900

생성물 1

HCID 66933221(1S,3S)-methyl 3-aminocyclopentanecarboxylate hydrochloride

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
0 °C

실험 절차

Acetyl chloride (3.5 mL, 49.3 mmol) was added dropwise at 0° C. to 100 mL of MeOH. The resulting mixture was stirred at 0° C. for 5 minutes before adding (1S,3S)-3-tert-butoxycarbonylamino-cyclopentanecarboxylic acid methyl ester (1.192 g, 5.2 mmol). The reaction mixture was allowed to warm up to RT and stirred for 48 h before being evaporated to give crude (1S,3S)-3-amino-cyclopentanecarboxylic acid methyl ester hydrochloride which was used as is in the following step.

후처리

  1. temperatureto warm up to RT
  2. stirringstirred for 48 h
  3. custombefore being evaporated

출처 및 근거

ORD 기록
ord-d0e4597c60774248a40955825ca9517d
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08012974B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트