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

Diethyl Ether → 1-[6-(Trifluoromethyl)pyridin-3-yl]ethan-1-one

HRID 1678062
노트
인쇄 미리보기

반응식

HRID 1678062 반응식
C[Mg+].[Br-].[F:4][C:5]([F:15])([F:14])[C:6]1[CH:13]=[CH:12][C:9](C#N)=[CH:8][N:7]=1.CC[O:18][CH2:19][CH3:20]>>[F:4][C:5]([F:15])([F:14])[C:6]1[N:7]=[CH:8][C:9]([C:19](=[O:18])[CH3:20])=[CH:12][CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 3283Diethyl Ether2회HCID 27775545-Cyano-2-(trifluoromethyl)pyridineHCID 178418689HCID 178418689, 화합물

생성물 1

HCID 218805781-[6-(Trifluoromethyl)pyridin-3-yl]ethan-1-one

실험 절차

A 3 M solution of MeMgBr in Et2O (7.2 mmol) was added to a stirred solution of 6-(trifluoromethyl)nicotinonitrile (0.82 g, 4.8 mmol) in ether (16 mL) dropwise over a 30 minute period. The reaction was stirred for 2 hours then the mixture was quenched with aqueous 1N HCl and extracted with Et2O. The organics were combined and washed with brine and dried over anhydrous MgSO4. The solvent was removed in vacuo yielding 530 mg of a brown solid.

후처리

  1. customthe mixture was quenched with aqueous 1N HCl
  2. extractionextracted with Et2O
  3. washwashed with brine
  4. dry with materialdried over anhydrous MgSO4
  5. customThe solvent was removed in vacuo

출처 및 근거

ORD 기록
ord-0607467a867240b985b8360d993b2414
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08008487B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트