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

m-Chloroperbenzoic acid → 1-[2-(4-Allyloxy-phenylmethanesulfinyl)-ethyl]-1H-[1,2,3]triazole

HRID 892250
노트
인쇄 미리보기

반응식

HRID 892250 반응식
[CH2:1]([O:4][C:5]1[CH:19]=[CH:18][C:8]([CH2:9][S:10][CH2:11][CH2:12][N:13]2[CH:17]=[CH:16][N:15]=[N:14]2)=[CH:7][CH:6]=1)[CH:2]=[CH2:3].ClC1C=C(C(OO)=[O:28])C=CC=1>ClCCl.C(OCC)(=O)C>[CH2:1]([O:4][C:5]1[CH:19]=[CH:18][C:8]([CH2:9][S:10]([CH2:11][CH2:12][N:13]2[CH:17]=[CH:16][N:15]=[N:14]2)=[O:28])=[CH:7][CH:6]=1)[CH:2]=[CH2:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 70297m-Chloroperbenzoic acidHCID 222420761-[2-(4-Allyloxy-benzylsulfanyl)-ethyl]-1H-[1,2,3]triazole

생성물 1

HCID 222420851-[2-(4-Allyloxy-phenylmethanesulfinyl)-ethyl]-1H-[1,2,3]triazole수율 62.2%

시약·촉매·용매 2

HCID 6344Dichloromethane용매HCID 8857Ethyl Acetate용매

실험 절차

To a solution of 1.90 g (6.9 mmol) 1-[2-(4-all yloxy-benzylsulfanyl)-ethyl]-1H-[1,2,3]triazole in 150 ml dichloromethane was added dropwise at −30° C. a solution of 1.86 g (8.3 mmol) 3-chloro-benzenecarboperoxoic acid in 40 ml ethyl acetate and stirring continued for 1 hour. The mixture was allowed to warm up over night, washed with sodium bicarbonate and sodium carbonate solution, then with water, dried and evaporated. Elution form silica with ethyl acetate/methanol 5:1 furnished 1.25 g (62%) 1-[2-(4-allyloxy-phenylmethanesulfinyl)-ethyl]-1H-[1,2,3]triazole as white solid.

후처리

  1. temperatureto warm up over night
  2. washwashed with sodium bicarbonate and sodium carbonate solution
  3. dry with materialwith water, dried
  4. customevaporated
  5. washElution
  6. customform silica with ethyl acetate/methanol 5:1

출처 및 근거

ORD 기록
ord-24a871f412714e10b75d2d71d232cf4d
출처 데이터셋
uspto-grants-2006_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07005526B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트