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

Aniline → 2-(Trifluoromethyl)quinoline

HRID 2215427
노트
인쇄 미리보기

반응식

HRID 2215427 반응식
CN(C)/[CH:3]=[CH:4]/[C:5](=O)[C:6]([F:9])([F:8])[F:7].FC(F)(F)C(OC(=O)C(F)(F)F)=O.[NH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>ClCCCl.C1(C)C(C)=CC=CC=1>[F:9][C:6]([F:7])([F:8])[C:5]1[CH:4]=[CH:3][C:31]2[C:26](=[CH:27][CH:28]=[CH:29][CH:30]=2)[N:25]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 6115AnilineHCID 9845Trifluoroacetic anhydrideHCID 2063589(3E)-4-(dimethylamino)-1,1,1-trifluorobut-3-en-2-one

생성물 1

HCID 27778052-(Trifluoromethyl)quinoline

시약·촉매·용매 2

HCID 111,2-Dichloroethane용매HCID 7237O-Xylene용매

실험 절차

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

According to instructions in the literature (Baraznenok, I. L., Nenajdenko, V. G., Balenkova, E. S. Eur. J. Org. Chem. 1999, 937–941), 1.2 g (7.18 mmol) of (E)-4-(dimethylamino)-1,1,1-trifluoro-3-buten-2-one is reacted with 2.03 g (7.18 mmol) of trifluoroacetic acid anhydride and 1.30 ml (14.36 mmol) of aniline in 72 ml of 1,2-dichloroethane, then in 36 ml of xylene. After working-up and purification on silica gel with hexane-ethyl acetate (0–100%), 1.01 g (71% of theory) of the product is obtained.

후처리

  1. custompurification on silica gel with hexane-ethyl acetate (0–100%), 1.01 g (71% of theory) of the product
  2. customis obtained

출처 및 근거

ORD 기록
ord-91bcca3662d14d98a4d3c15fbda5f025
출처 데이터셋
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07109212B2

반응 노트

불러오는 중…