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

2-methylthio-5-trifluoromethyl-1H-indole → 5-(trifluoromethyl)-1H-indole

HRID 1371942
노트
인쇄 미리보기

반응식

HRID 1371942 반응식
CS[C:3]1[NH:4][C:5]2[C:10]([CH:11]=1)=[CH:9][C:8]([C:12]([F:15])([F:14])[F:13])=[CH:7][CH:6]=2>[Ni].C(O)C>[F:15][C:12]([F:13])([F:14])[C:8]1[CH:9]=[C:10]2[C:5](=[CH:6][CH:7]=1)[NH:4][CH:3]=[CH:11]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 210714332-methylthio-5-trifluoromethyl-1H-indole

생성물 1

HCID 27630755-(trifluoromethyl)-1H-indole

시약·촉매·용매 2

HCID 935Nickel촉매HCID 702Ethanol용매

실험 절차

Combine moist Raney nickel (330 g), 2-methylthio-5-trifluoromethyl-1H-indole (33.8 g, 146.2 mmol) and absolute ethanol (850 ml) and stir. After 1.5 hours, filter the mixture through celite and wash the celite with ethanol (500 ml). Evaporate the filtrate to dryness, add toluene (20 ml) and evaporate and dry to give 5-trifluoromethylindole: mp=55–60° C.

후처리

  1. filtrationfilter the mixture through celite
  2. washwash the celite with ethanol (500 ml)
  3. customEvaporate the filtrate to dryness
  4. additionadd toluene (20 ml)
  5. customevaporate
  6. customdry

출처 및 근거

ORD 기록
ord-de4e169c35db4b5d968949cc7017f7e7
출처 데이터셋
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07157488B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트