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Toluene → 1,1,6-Trimethyl-4-(propan-2-yl)-1,2,3,4-tetrahydronaphthalene

HRID 979756
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인쇄 미리보기

반응식

HRID 979756 반응식
[C:1]1([CH3:7])[CH:6]=[CH:5]C=[CH:3][CH:2]=1.[CH3:8][C:9](O)([CH2:11][CH2:12][CH:13]=[C:14]([CH3:16])[CH3:15])[CH3:10].[CH3:18]CCCCC>>[CH:14]([CH:13]1[C:5]2[C:8](=[CH:3][CH:2]=[C:1]([CH3:7])[CH:6]=2)[C:9]([CH3:10])([CH3:18])[CH2:11][CH2:12]1)([CH3:16])[CH3:15]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 1140TolueneHCID 8058HexaneHCID 801835-Hepten-2-ol, 2,6-dimethyl-

생성물 1

HCID 2264181,1,6-Trimethyl-4-(propan-2-yl)-1,2,3,4-tetrahydronaphthalene

반응 조건

온도
10 °C

실험 절차

1050 g of sulphuric acid are provided and a mixture of 1.5 l of toluene and 497 g of 2,6-dimethyl-hept-5-en-2-ol are added dropwise during 35 minutes while cooling (10° C.). The mixture is stirred at room temperature for 1.5 hours. The mixture is now diluted with hexane, poured on to ice, washed neutral, dried and evaporated. After distillation there are obtained 455 g of 1-isopropyl-4,4,7-trimethyl-1,2,3,4-tetrahydro-naphthalene (purity 75%).

후처리

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
  1. additionare added dropwise during 35 minutes
  2. additionpoured on to ice
  3. washwashed neutral
  4. customdried
  5. customevaporated
  6. distillationAfter distillation

출처 및 근거

ORD 기록
ord-87fa37a644f14e95a7e4c093549cc9ad
출처 데이터셋
uspto-grants-1987_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04634548

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