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

Thionyl Chloride → 4-(Chloromethyl)quinoline--hydrogen chloride (1/1)

HRID 1729096
노트
인쇄 미리보기

반응식

HRID 1729096 반응식
Br.O[CH2:3][C:4]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[N:7]=[CH:6][CH:5]=1.S(Cl)([Cl:16])=O>>[ClH:16].[Cl:16][CH2:3][C:4]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[N:7]=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24386Thionyl ChlorideHCID 19013536Quinolin-4-ylmethanol hydrobromide

생성물 1

HCID 230016194-(Chloromethyl)quinoline--hydrogen chloride (1/1)수율 80.7%

실험 절차

A reaction mixture of 4-(hydroxymethyl)-quinoline hydrobromide (2.0 g, 12.6mmol) and thionylchloride (20 mL) was heated to reflux for 2 hours. This was allowed to cool and then concentrated in vacuum. The green solid was treated with ethyl ether, filtered, washed with ethyl ether and dried in vacuum to yield 4-(chloromethyl)-quinoline hydrochloride (2.17 g, 80.7%).

후처리

  1. temperaturewas heated
  2. temperatureto reflux for 2 hours
  3. temperatureto cool
  4. concentrationconcentrated in vacuum
  5. additionThe green solid was treated with ethyl ether
  6. filtrationfiltered
  7. washwashed with ethyl ether
  8. customdried in vacuum

출처 및 근거

ORD 기록
ord-9b6a0e8d643b48079adb7a744577a24d
출처 데이터셋
uspto-grants-1994_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05331006

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트