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

4-(5-Cyclopropylamino-8,8-dimethyl-5,6,7,8-tetrahydro-naphthalene-2-ylethynyl)-benzoic acid ethyl ester → 6-Bromo-8-vinyl-2,2,4,4-tetramethyl-chroman

HRID 381045
노트
인쇄 미리보기

반응식

HRID 381045 반응식
[CH2:1](OC(=O)C1C=CC(C#CC2C=CC3C(NC4CC4)CCC(C)(C)C=3C=2)=CC=1)C.[Br:30][C:31]1[CH:32]=[C:33]2[C:38](=[C:39]([CH:41]=O)[CH:40]=1)[O:37][C:36]([CH3:44])([CH3:43])[CH2:35][C:34]2([CH3:46])[CH3:45]>CCCCCC>[Br:30][C:31]1[CH:32]=[C:33]2[C:38](=[C:39]([CH:41]=[CH2:1])[CH:40]=1)[O:37][C:36]([CH3:44])([CH3:43])[CH2:35][C:34]2([CH3:46])[CH3:45]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 129717084-(5-Cyclopropylamino-8,8-dimethyl-5,6,7,8-tetrahydro-naphthalene-2-ylethynyl)-benzoic acid ethyl ester2회HCID 225689466-Bromo-2,2,4,4-tetramethyl chroman-8-carbaldehyde2회

생성물 1

HCID 225689226-Bromo-8-vinyl-2,2,4,4-tetramethyl-chroman수율 72%

시약·촉매·용매 1

HCID 8058Hexane용매

실험 절차

A solution of methylidene triphenyl phosphorane [generated from methyl triphenylphosphonium bromide (7 g, 20 mmol) and (11.8 mL, 19 mmol) of a 1 .6M solution of n-butyl lithium in hexanes] was added 6-bromo-2,2,4,4-tetramethyl chroman-8-carbaldehyde (Intermediate 30, 0.52 g, 1.75 mmol). After 1 h the reaction mixture was diluted with hexane, washed with brine (×1), dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to a clear oil which was subjected to flash column chromatography over silica gel (230-400 mesh) using 2% ethyl acetate in hexane as the eluent to afford the title compound as a clear oil (0.37 g, 72%).

후처리

  1. washwashed with brine (×1)
  2. dry with materialdried over anhydrous sodium sulfate
  3. filtrationfiltered
  4. customevaporated in vacuo to a clear oil which

출처 및 근거

ORD 기록
ord-569bd1803482404f9f8d5e5557063fa1
출처 데이터셋
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06303785B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트