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

Triethylamine → 3-Bromo-6-chloro-4-methylpyridine-2-carbonitrile

HRID 340239
노트
인쇄 미리보기

반응식

HRID 340239 반응식
[Br:1][C:2]1[C:3]([CH3:10])=[CH:4][C:5]([Cl:9])=[N+:6]([O-])[CH:7]=1.[Si]([C:15]#[N:16])(C)(C)C.C(N(CC)CC)C>C(#N)C>[Br:1][C:2]1[C:7]([C:15]#[N:16])=[N:6][C:5]([Cl:9])=[CH:4][C:3]=1[CH3:10]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 82115Trimethylsilyl cyanideHCID 866523465-Bromo-2-chloro-4-methylpyridine 1-oxide

생성물 1

HCID 866523473-Bromo-6-chloro-4-methylpyridine-2-carbonitrile

시약·촉매·용매 1

HCID 6342Acetonitrile용매

반응 조건

온도
100 °C

실험 절차

To a solution of 5-bromo-2-chloro-4-methylpyridine 1-oxide (from step 1) (1.0 eq.) in acetonitrile (0.2 M) was added TMSCN (4.0 eq.) and triethylamine (3.0 eq.). The reaction was heated at 100° C. overnight. After cooling to room temperature, the solvent was concentrated en vacuo, and the residue was purified by a COMBIFLASH® system (ISCO) using 0-50% ethyl acetate in hexane to give 3-bromo-6-chloro-4-methylpicolinonitrile.

후처리

  1. temperatureAfter cooling to room temperature
  2. concentrationthe solvent was concentrated en vacuo
  3. customthe residue was purified by a COMBIFLASH® system (ISCO)

출처 및 근거

ORD 기록
ord-f51ec58fbb9540f1b9c383f14a4cb579
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08895577B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트