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

Toluene → 4-Bromo-3,5-dimethylpyridine

HRID 75236
노트
인쇄 미리보기

반응식

HRID 75236 반응식
[Br:1][C:2]1[C:7]([CH3:8])=[CH:6][N+:5]([O-])=[CH:4][C:3]=1[CH3:10].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(C)C=CC=CC=1>C(OCC)(=O)C>[Br:1][C:2]1[C:7]([CH3:8])=[CH:6][N:5]=[CH:4][C:3]=1[CH3:10]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1140TolueneHCID 11776TriphenylphosphineHCID 124930364-Bromo-3,5-dimethylpyridin-1-ium-1-olate

생성물 1

HCID 223232464-Bromo-3,5-dimethylpyridine수율 38%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

반응 조건

온도
180 °C

실험 절차

To a microwave tube was added 4-bromo-3,5-dimethylpyridine 1-oxide (2.00 g, 9.90 mmol), triphenylphosphine (3.12 g, 11.9 mmol) and toluene (10 mL). The tube was sealed and heated at 180° C. overnight. The reaction solution was diluted with ethyl acetate, and filtered. The filtrate was concentrated and purified by flash chromatography (10% to 40% ethyl acetate in hexanes) to afford the desired product as a yellow oil (700 mg, 38%). 1H NMR (400 MHz, CDCl3): δ 8.22 (s, 2 H), 2.38 (s, 6 H); LCMS calculated for C7H9BrN(M+H)+: m/z=186.0.

후처리

  1. customThe tube was sealed
  2. filtrationfiltered
  3. concentrationThe filtrate was concentrated
  4. custompurified by flash chromatography (10% to 40% ethyl acetate in hexanes)

출처 및 근거

ORD 기록
ord-cf7958424b63469085f6a1986694f0c3
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08835423B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트