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

Hydrochloric Acid → HCID 23000956, 화합물

HRID 397720
노트
인쇄 미리보기

반응식

HRID 397720 반응식
[CH3:1][C:2]1([CH3:11])[CH2:7][CH2:6][CH:5]([CH2:8][CH2:9][OH:10])[CH2:4][CH2:3]1.[Br:12][C:13]1[CH:18]=[CH:17][C:16]([S:19](Cl)(=[O:21])=[O:20])=[CH:15][CH:14]=1.C(N(CC)CC)C.Cl>ClCCl>[Br:12][C:13]1[CH:18]=[CH:17][C:16]([S:19]([O:10][CH2:9][CH2:8][CH:5]2[CH2:4][CH2:3][C:2]([CH3:11])([CH3:1])[CH2:7][CH2:6]2)(=[O:21])=[O:20])=[CH:15][CH:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 7396p-Bromobenzenesulfonyl chloride2회HCID 8471Triethylamine2회HCID 149767172-(4,4-Dimethylcyclohexyl)ethan-1-ol

생성물 1

HCID 23000956HCID 23000956, 화합물수율 13.3%

시약·촉매·용매 1

HCID 6344
Dichloromethane
용매

실험 절차

To a solution of 2-(4,4-dimethylcyclohexyl)-1-ethanol (Preparation 15, 1.45 g, 9 mmol) and 4-bromobenzenesulfonyl chloride (2.53 g, 10 mmol) in dichloromethane (30 ml) was added triethylamine (1.9 ml, 13.5 mmol), and the reaction mixture was allowed to stir at room temperature for 24 h. After a further addition of 4-bromobenzenesulfonyl chloride (2.53 g, 10 mmol) and triethylamine (1.9 ml, 13.5 mmol), the reaction mixture was heated under reflux for 1 h. After allowing the reaction mixture to cool to room temperature, the mixture was treated with 2N aqueous hydrochloric acid (100 ml) and the phases were separated. The organic extract was dried (MgSO4), filtered and concentrated in vacuo to afford the crude product. The residue was purified by silica (80 g) column chromatography eluting with diethyl ether:hexane (1:20) to give the title compound as a colourless oil (450 mg, 13%).

후처리

  1. temperaturethe reaction mixture was heated
  2. temperatureunder reflux for 1 h
  3. temperatureto cool to room temperature
  4. customthe phases were separated
  5. extractionThe organic extract
  6. dry with materialwas dried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customto afford the crude product
  10. customThe residue was purified by silica (80 g) column chromatography
  11. washeluting with diethyl ether:hexane (1:20)

출처 및 근거

ORD 기록
ord-a8317c365adc4ad6af9c9e1fd172afe1
출처 데이터셋
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06610711B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트