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

Sodium Hydroxide → 5-(6-Fluoro-1H-indol-5-yl)-pent-4-yn-1-ol

HRID 2212548
노트
인쇄 미리보기

반응식

HRID 2212548 반응식
C(OC([N:8]1[C:16]2[C:11](=[CH:12][C:13]([C:18]#[C:19][CH2:20][CH2:21][CH2:22][OH:23])=[C:14]([F:17])[CH:15]=2)[CH:10]=[CH:9]1)=O)(C)(C)C.[OH-].[Na+]>CCO>[F:17][C:14]1[CH:15]=[C:16]2[C:11]([CH:10]=[CH:9][NH:8]2)=[CH:12][C:13]=1[C:18]#[C:19][CH2:20][CH2:21][CH2:22][OH:23]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 695149406-Fluoro-5-(5-hydroxy-pent-1-ynyl)-indole-1-carboxylic acid tert-butyl ester

생성물 1

HCID 219666015-(6-Fluoro-1H-indol-5-yl)-pent-4-yn-1-ol수율 843.9%

시약·촉매·용매 1

HCID 702Ethanol용매

반응 조건

온도
60 °C

실험 절차

A solution of 950 mg (0.3 mmol) 6-Fluoro-5-(5-hydroxy-pent-1-ynyl)-indole-1-carboxylic acid tert-butyl ester in 20 ml EtOH was treated with 2 ml of saturated aqeous NaOH and stirred during 2 hours at 60° C. 75% of the solvent were evaporated, the resulting mixture was poured into 5 ml of water, acidified with 2M aqueous HCl, and extracted with EtOAc. Drying of the combined organic layers with MgSO4, evaporation of the solvent, and chromatography on silica gel with CH2Cl2 gave 550 mg (84%) of 5-(6-Fluoro-1H-indol-5-yl)-pent-4-yn-1-ol as a viscous light yellow oil, MS: 218 (M).

후처리

  1. custom75% of the solvent were evaporated
  2. additionthe resulting mixture was poured into 5 ml of water
  3. extractionextracted with EtOAc
  4. dry with materialDrying of the combined organic layers with MgSO4, evaporation of the solvent, and chromatography on silica gel with CH2Cl2

출처 및 근거

ORD 기록
ord-ba7b9d8b0040448e85904e4b0125ec39
출처 데이터셋
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07102007B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트