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

1,4-Butane sultone → HCID 178448552, 화합물

HRID 239196
노트
인쇄 미리보기

반응식

HRID 239196 반응식
[Cl-:1].[CH2:2]([N+:6]1[CH:10]=[CH:9][N:8]([CH3:11])[CH:7]=1)[CH2:3][CH2:4][CH3:5].[CH2:12]1[CH2:19][O:18][S:15](=[O:17])(=[O:16])[CH2:14][CH2:13]1>>[Cl:1][CH2:19][CH2:12][CH2:13][CH2:14][S:15]([O-:18])(=[O:17])=[O:16].[CH2:2]([N+:6]1[CH:10]=[CH:9][N:8]([CH3:11])[CH:7]=1)[CH2:3][CH2:4][CH3:5]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 154111,4-Butane sultoneHCID 178448538HCID 178448538, 화합물

생성물 1

HCID 178448552HCID 178448552, 화합물

반응 조건

온도
40 °C

실험 절차

The mixture of equivalent of 1-butyl-3-methylimidazolium chloride and 20 equivalents of 1,4-butane sultone is stirred at 40° C. (temperature in the oil-bath) for 24 hours). The excess of 1,4-butane sultone was distilled off in vacuum and the residue was dried overnight at 50° C. in high vacuum (1·10−3mbar). Liquid 1-butyl-3-methylimidazolium 4-chlorobutylsulfonate is obtained in close to quantitative yield. The material was characterized by NMR spectroscopy.

후처리

  1. distillationThe excess of 1,4-butane sultone was distilled off in vacuum
  2. customthe residue was dried overnight at 50° C. in high vacuum (1·10−3mbar)

출처 및 근거

ORD 기록
ord-018438cc317543bf8e7826b3dcfb6418
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08642778B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트