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

Benzene → 3-[4-(Trifluoromethyl)phenyl]-2-propynal

HRID 381445
노트
인쇄 미리보기

반응식

HRID 381445 반응식
[F:1][C:2]([F:14])([F:13])[C:3]1[CH:8]=[CH:7][C:6]([C:9]#[C:10][CH2:11][OH:12])=[CH:5][CH:4]=1.CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O.C1C=CC=CC=1>C(Cl)Cl>[F:1][C:2]([F:13])([F:14])[C:3]1[CH:4]=[CH:5][C:6]([C:9]#[C:10][CH:11]=[O:12])=[CH:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 241BenzeneHCID 159087TriacetoxyperiodinaneHCID 118304283-(4-(Trifluoromethyl)phenyl)prop-2-yn-1-ol

생성물 1

HCID 183633083-[4-(Trifluoromethyl)phenyl]-2-propynal수율 84%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

In 20 ml of methylene chloride were dissolved 2.21 g (11.0 mmol) of 3-[4-(trifluoromethyl)phenyl]-2-propyn-1-ol, and 7.43 g (17.5 mmol) of Dess-Martin reagent were added to the solution under ice-cooling for 1.7 hours. Benzene was added to the resulting mixture and the insolubles were removed by filtration, followed by concentration of the filtrate to obtain 1.83 g (yield: 84%) of the title compound as an oil.

후처리

  1. additionwere added to the solution under ice-
  2. temperaturecooling for 1.7 hours
  3. customthe insolubles were removed by filtration

출처 및 근거

ORD 기록
ord-f62bd9873b784634b33abc45487c57d9
출처 데이터셋
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06306880B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트