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

Anisole → 6-Methoxy-1,1,4,4-tetramethyl-2,3-dihydronaphthalene

HRID 1883263
노트
인쇄 미리보기

반응식

HRID 1883263 반응식
Cl[C:2]([CH3:10])([CH2:4][CH2:5][C:6](Cl)([CH3:8])[CH3:7])[CH3:3].[C:11]1([O:17][CH3:18])[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.[Al+3].[Cl-].[Cl-].[Cl-]>>[CH3:18][O:17][C:11]1[CH:16]=[C:15]2[C:14](=[CH:13][CH:12]=1)[C:6]([CH3:8])([CH3:7])[CH2:5][CH2:4][C:2]2([CH3:10])[CH3:3]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 7519AnisoleHCID 80360Hexane, 2,5-dichloro-2,5-dimethyl-2회HCID 6451240Aluminum(III) Chloride

생성물 1

HCID 103310036-Methoxy-1,1,4,4-tetramethyl-2,3-dihydronaphthalene

반응 조건

온도
0 °C

실험 절차

To a solution of 2,5-dichloro-2,5-dimethyl-hexane (Intermediate 1, 25.3 g, 0.14 mol) in anisole (60 mL, 0.55 mol) at 0° C. was added AlCl3 (18.4 g, 0.14 mmol) portionwise. After stirring for 2 h at 0° C., the mixture was poured onto ice and extracted with hexane. The organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo. The excess anisole was removed by vacuum distillation and the title compound was obtained as a white solid upon cooling (30.5 g, 100%).

후처리

  1. additionthe mixture was poured onto ice
  2. extractionextracted with hexane
  3. washThe organic layer was washed with brine
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated in vacuo
  6. customThe excess anisole was removed by vacuum distillation

출처 및 근거

ORD 기록
ord-0bb82593d2a4451c96de01d9481c4f3f
출처 데이터셋
uspto-grants-2004_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06759547B1

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트