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

7-Benzyloxy-4-chloro-6-methoxyquinoline hydrochloride → 4-Chloro-6-methoxyquinolin-7-ol

HRID 393598
노트
인쇄 미리보기

반응식

HRID 393598 반응식
Cl.C([O:9][C:10]1[CH:19]=[C:18]2[C:13]([C:14]([Cl:20])=[CH:15][CH:16]=[N:17]2)=[CH:12][C:11]=1[O:21][CH3:22])C1C=CC=CC=1>C(O)(C(F)(F)F)=O>[Cl:20][C:14]1[C:13]2[C:18](=[CH:19][C:10]([OH:9])=[C:11]([O:21][CH3:22])[CH:12]=2)[N:17]=[CH:16][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 226465617-Benzyloxy-4-chloro-6-methoxyquinoline hydrochloride

생성물 1

HCID 1355837314-Chloro-6-methoxyquinolin-7-ol수율 98%

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

A solution of 7-benzyloxy-4-chloro-6-methoxyquinoline hydrochloride (6.8 g, 20 mmol) in TFA (80 ml) was heated at reflux for 5.5 hours. The volatiles were removed by evaporation, the residue suspended in water and the mixture was adjusted to pH7 with a saturated aqueous sodium hydrogen carbonate solution. The resulting solid was collected by filtration, washed with water, ether and dried under vacuum to give 4-chloro-7-hydroxy-6-methoxyquinoline (4.1 g, 98%).

후처리

  1. temperatureat reflux for 5.5 hours
  2. customThe volatiles were removed by evaporation
  3. filtrationThe resulting solid was collected by filtration
  4. washwashed with water, ether
  5. customdried under vacuum

출처 및 근거

ORD 기록
ord-a07b263e1f9c44569f87333c7a7d219b
출처 데이터셋
uspto-grants-2004_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06809097B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트