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

HCID 22121731, 화합물 → 2-[2-fluoro-4-((1S,2S)-2-hydroxycyclo-pentylthio)phenyl]propionic acid

HRID 1506866
노트
인쇄 미리보기

반응식

HRID 1506866 반응식
[O:1]1[C:3]2[CH2:4][CH2:5][CH2:6][C:2]1=2.[F:7][C:8]1[CH:13]=[C:12]([SH:14])[CH:11]=[CH:10][C:9]=1[CH:15]([CH3:20])[C:16]([O:18]C)=[O:17]>ClCCl>[F:7][C:8]1[CH:13]=[C:12]([S:14][C@H:2]2[CH2:6][CH2:5][CH2:4][C@@H:3]2[OH:1])[CH:11]=[CH:10][C:9]=1[CH:15]([CH3:20])[C:16]([OH:18])=[O:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 22121731HCID 22121731, 화합물HCID 60155350Methyl 2-(2-fluoro-4-mercaptophenyl)propionate

생성물 1

HCID 601553552-[2-fluoro-4-((1S,2S)-2-hydroxycyclo-pentylthio)phenyl]propionic acid수율 84%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To an aqueous solution (19 mL) of borax (0.1 g, 0.26 mmol), 1,2-epoxycyclopentene (0.8 mL, 9.3 mmol) and compound (9) (1.60 g, 7.5 mmol) were sequentially added. The mixture was stirred at room temperature for 39 hours and dichloromethane (50 mL) was added thereto. The organic layer was washed with water and dried (over sodium sulfate). The solvent was distilled off, and the residue was subjected to silica gel column chromatography and elution with an n-hexane/ethyl acetate (8:1) solution followed by conventional hydrolysis to give 1.79 g (84%) of compound (16) of interest as yellow oil.

후처리

  1. washThe organic layer was washed with water
  2. dry with materialdried (over sodium sulfate)
  3. distillationThe solvent was distilled off
  4. washthe residue was subjected to silica gel column chromatography and elution with an n-hexane/ethyl acetate (8:1) solution
  5. customfollowed by conventional hydrolysis

출처 및 근거

ORD 기록
ord-c551d5d5140741bd810d2a6971460d73
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09221786B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트