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

Triethylamine → cis-1,4-Bis-(methylsulfonyloxy)-but-2-ene

HRID 2216353
노트
인쇄 미리보기

반응식

HRID 2216353 반응식
[CH3:1][S:2](Cl)(=[O:4])=[O:3].[CH2:6]([OH:11])/[CH:7]=[CH:8]\[CH2:9][OH:10].C(N(CC)CC)C>C(OCC)(=O)C>[CH3:1][S:2]([O:10][CH2:9]/[CH:8]=[CH:7]\[CH2:6][O:11][S:2]([CH3:1])(=[O:4])=[O:3])(=[O:4])=[O:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 31297Methanesulfonyl chlorideHCID 6437902-Butene-1,4-diol, (2Z)-

생성물 1

HCID 6433331cis-1,4-Bis-(methylsulfonyloxy)-but-2-ene

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

In an ice bath, 26 ml of methanesulfonyl chloride was added dropwise in to a mixture of 10 g of cis-2-buten-1,4-diol, 63 ml of triethylamine and 1000 ml of ethyl acetate, followed by stirring at the same temperature for 3 hours. Then, the insoluble matters were removed by filtration. The filtrate was further filtered through silica gel and washed with ethyl acetate. Then, the filtrate was evaporated, to give 21.4 g of cis-1,4-bis(methanesulfonyloxy)-2-butene.

후처리

  1. customThen, the insoluble matters were removed by filtration
  2. filtrationThe filtrate was further filtered through silica gel
  3. washwashed with ethyl acetate
  4. customThen, the filtrate was evaporated

출처 및 근거

ORD 기록
ord-0e0d9f1eeeec46699110412446c8b6b0
출처 데이터셋
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07112593B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트