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

Sodium hydride → 3-(2-Chloro-phenylsulfanyl)-cyclopentanecarboxylic acid methyl ester

HRID 1367472
노트
인쇄 미리보기

반응식

HRID 1367472 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[SH:8].[H-].[Na+].[CH3:11][O:12][C:13]([CH:15]1[CH2:19][CH2:18][CH:17](OS(C)(=O)=O)[CH2:16]1)=[O:14]>C1COCC1>[CH3:11][O:12][C:13]([CH:15]1[CH2:19][CH2:18][CH:17]([S:8][C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[Cl:1])[CH2:16]1)=[O:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 24758Sodium hydrideHCID 80599o-ChlorothiophenolHCID 205054773-(Methoxycarbonyl)cyclopentyl methanesulfonate

생성물 1

HCID 669185443-(2-Chloro-phenylsulfanyl)-cyclopentanecarboxylic acid methyl ester

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of 2-chlorothiophenol (0.19 g, 1.5 eq) in THF (6.0 mL) was treated with NaH (60% dispersion in mineral oil, 0.05 g, 1.5 eq). The resulting solution was stirred at RT for 30 min. A solution of 3-methanesulfonyloxy-cyclopentanecarboxylic acid methyl ester (0.20 g, 1.0 eq) in THF (2.0 mL) was then added dropwise. The mixture was warmed at 50° C. and stirred for 3 h. The mixture was partitioned between 1N sodium bicarbonate and ethyl acetate. The combined organic phases were dried over sodium sulfate and evaporated. The title compound was obtained as a colorless oil (0.24 g, 98%) and was used without further purification in the next step. MS (ESI): m/z=271.2 [M+H]+.

후처리

  1. temperatureThe mixture was warmed at 50° C.
  2. stirringstirred for 3 h
  3. customThe mixture was partitioned between 1N sodium bicarbonate and ethyl acetate
  4. dry with materialThe combined organic phases were dried over sodium sulfate
  5. customevaporated

출처 및 근거

ORD 기록
ord-1cca34fc6500435a9c2a892dee461348
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07893099B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트