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

Sodium Hydroxide → 8-Bromo-3-methyl-5,6,7,8-tetrahydroquinoline

HRID 649175
노트
인쇄 미리보기

반응식

HRID 649175 반응식
[CH3:1][C:2]1[CH:3]=[N:4][C:5]2[CH:6](O)[CH2:7][CH2:8][CH2:9][C:10]=2[CH:11]=1.P(Br)(Br)[Br:14].[OH-].[Na+]>C(Cl)(Cl)Cl>[CH3:1][C:2]1[CH:3]=[N:4][C:5]2[CH:6]([Br:14])[CH2:7][CH2:8][CH2:9][C:10]=2[CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 24614Phosphorus tribromideHCID 123582223-Methyl-5,6,7,8-tetrahydroquinolin-8-ol

생성물 1

HCID 139602608-Bromo-3-methyl-5,6,7,8-tetrahydroquinoline

시약·촉매·용매 1

HCID 6212Chloroform용매2회

실험 절차

1.50 Grams of 3-methyl-8-hydroxy-5,6,7,8-tetrahydroquinoline was dissolved in 20 ml of chloroform, to this solution was added dropwise a solution consisting of 1.35 g of phosphorus tribromide and 5 ml of chloroform under ice-cooled condition, then the mixture was stirred under ice-cooled condition for 2 hours, next was stirred at room temperature overnight. To the reaction mixture was added 5%-sodium hydroxide aqueous solution, then was extracted with chloroform. The chloroform layer was washed with an aqueous solution saturated with sodium chloride, and dried with anhydrous magnesium sulfate. The solvent was removed by evaporation to obtain 1.80 g of 3-methyl-8-bromo-5,6,7,8-tetrahydroquinoline.

후처리

  1. additionwas added dropwise a solution
  2. temperaturecooled condition
  3. temperaturecooled condition for 2 hours
  4. stirringnext was stirred at room temperature overnight
  5. extractionwas extracted with chloroform
  6. washThe chloroform layer was washed with an aqueous solution saturated with sodium chloride
  7. dry with materialdried with anhydrous magnesium sulfate
  8. customThe solvent was removed by evaporation

출처 및 근거

ORD 기록
ord-ba5ce626a49346099c909ad07942421c
출처 데이터셋
uspto-grants-1988_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04738970

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트