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

Benzyl Chloride → 2-(Benzyloxy)-4,6-dimethylnicotinonitrile

HRID 577463
노트
인쇄 미리보기

반응식

HRID 577463 반응식
[OH:1][C:2]1[N:9]=[C:8]([CH3:10])[CH:7]=[C:6]([CH3:11])[C:3]=1[C:4]#[N:5].[CH2:12](Cl)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>[Ag-]=O.C1(C)C=CC=CC=1>[CH2:12]([O:1][C:2]1[N:9]=[C:8]([CH3:10])[CH:7]=[C:6]([CH3:11])[C:3]=1[C:4]#[N:5])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 7503Benzyl ChlorideHCID 178425241HCID 178425241, 화합물

생성물 1

HCID 229349272-(Benzyloxy)-4,6-dimethylnicotinonitrile수율 94.4%

시약·촉매·용매 2

HCID 178418778HCID 178418778, 화합물촉매HCID 1140Toluene용매

반응 조건

온도
110 °C

실험 절차

A mixture of 2-hydroxy-4,6-dimethylnicotinonitrile (5.3 g, 36 mmol), benzyl chloride (5.7 mL, 45 mmol), silver(I)oxide (9.2 g, 40 mmol) and toluene (50 mL) were heated at 110° C. in a sealed tube for 20 hours. The mixture was cooled to room temperature and the solids were filtered and rinsed with dichloromethane. The filtrate was concentrated under vacuum and purified by column chromatography (40% EtOAc/Heptane) to give 2-(benzyloxy)-4,6-dimethylnicotinonitrile (Cpd II, 8.1 g, 94% yield) as a white solid.

후처리

  1. temperatureThe mixture was cooled to room temperature
  2. filtrationthe solids were filtered
  3. washrinsed with dichloromethane
  4. concentrationThe filtrate was concentrated under vacuum
  5. custompurified by column chromatography (40% EtOAc/Heptane)

출처 및 근거

ORD 기록
ord-fbdea4f4fbf44429b994552a19fab072
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09040515B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트