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

Dimethylformamide → 61350-60-5

HRID 2258492
노트
인쇄 미리보기

반응식

HRID 2258492 반응식
[N:1]1([C:9]([O:11][CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[O:10])[CH2:8][CH2:7][CH2:6][C@H:2]1[C:3](O)=[O:4].CN(C=O)C.C(Cl)(=O)C([Cl:27])=O>C(Cl)Cl>[C:9]([N:1]1[CH2:8][CH2:7][CH2:6][C@H:2]1[C:3]([Cl:27])=[O:4])([O:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 65578Oxalyl chlorideHCID 101987Benzyloxycarbonyl-L-proline

생성물 1

HCID 1103285461350-60-5

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a stirred solution of CBZ-L-Pro-OH (0.62 g, 2.49 mmol) and a drop of DMF in methylene chloride (10 ml) under argon was added oxalyl chloride (0.26 ml; 2.99 mmol) which resulted in a vigorous evolution of gas. After the evolution of gas ceased, the reaction was stirred for an additional 30 minutes. The reaction was then concentrated to give, as a light yellow oil, N-carbobenzoxy-L-prolyl chloride (CBZ-L-Pro-Cl).

후처리

  1. customresulted in a vigorous evolution of gas
  2. concentrationThe reaction was then concentrated

출처 및 근거

ORD 기록
ord-d2d0cf91f59943f0b8086afeff3628b3
출처 데이터셋
uspto-grants-1997_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05661167

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트