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

3-Trifluoromethylisobutyranilide → Ethyl-N-(3-trifluoromethylphenyl)isobutyrimidate

HRID 1658671
노트
인쇄 미리보기

반응식

HRID 1658671 반응식
[B-](F)(F)(F)F.[CH3:6][CH2:7][O+](CC)CC.[F:13][C:14]([F:28])([F:27])[C:15]1[CH:16]=[C:17]([CH:24]=[CH:25][CH:26]=1)[NH:18][C:19](=[O:23])[CH:20]([CH3:22])[CH3:21]>ClCCl>[CH2:6]([O:23][C:19](=[N:18][C:17]1[CH:24]=[CH:25][CH:26]=[C:15]([C:14]([F:27])([F:28])[F:13])[CH:16]=1)[CH:20]([CH3:22])[CH3:21])[CH3:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1372643-TrifluoromethylisobutyranilideHCID 2723982Triethyloxonium tetrafluoroborate

생성물 1

HCID 21528116Ethyl-N-(3-trifluoromethylphenyl)isobutyrimidate

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

Add a solution of 5.0 g. (0.03 moles) of triethyloxonium fluoborate in 13 ml. of dichloromethane to a solution of 7.3 g. (0.03 moles) of 3'-trifluoromethylisobutyranilide in 60 ml. of dichloromethane and reflux for 20 hours. Remove 50 ml. of dichloromethane and add 150 ml. of dry ether to precipitate out the product of this example as its fluoborate salt, m.p.=95°-100°C.

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. additionAdd a solution of 5.0 g
  2. customRemove 50 ml
  3. additionof dichloromethane and add 150 ml
  4. customof dry ether to precipitate out the product of this example as its fluoborate salt, m.p.=95°-100°C.

출처 및 근거

ORD 기록
ord-9ca430cf61254486bff17b0e0f712086
출처 데이터셋
uspto-grants-1976_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03965176

반응 노트

불러오는 중…