Benzylamine → 4,6-dimethyl-7-hydroxy-1-benzylamino-2-phenyl-3H-indene

HRID 2232201노트

반응식

HRID 2232201 반응식
[CH3:1][C:2]1[CH:10]=[C:9]([CH3:11])[C:8]([OH:12])=[C:7]2[C:3]=1[CH2:4][CH:5]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[C:6]2=O.[CH2:20]([NH2:27])[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>C(OCC)C.ClCCl>[CH3:1][C:2]1[CH:10]=[C:9]([CH3:11])[C:8]([OH:12])=[C:7]2[C:3]=1[CH2:4][C:5]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[C:6]2[NH:27][CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1

참가 물질

5

반응물 2

HCID 7504BenzylamineHCID 140302654,6-Dimethyl-7-hydroxy-2-phenyl-1-indanone

생성물 1

HCID 150452594,6-dimethyl-7-hydroxy-1-benzylamino-2-phenyl-3H-indene

시약·촉매·용매 2

HCID 3283Diethyl Ether용매2회HCID 6344Dichloromethane용매

실험 절차

5.0 Grams of 4,6-dimethyl-7-hydroxy-2-phenyl-1-indanone was dissolved in 10 ml of diethyl ether and 10 ml of dichloromethane, then this solution was added dropwise gradually to a mixture of a solution of 2.55 ml of benzylamine in 10 ml of diethyl ether with 8 g of Molecular sieves 5A. The whole mixture was stirred at room temperature for 2 days and filtered by using Celite to obtain filtrate. The Celite used was washed with dichloromethane and ethanol, then these washing liquors were combihed with the above-mentioned filtrate and concentrated. Recrystallized from dichloromethane-ethanol to obtain 3.83 g of 4,6-dimethyl-7-hydroxy-1-benzylamino-2-phenyl-3H-indene. Orange needle-like crystals.

후처리

  1. filtrationfiltered
  2. customto obtain filtrate
  3. washThe Celite used was washed with dichloromethane and ethanol
  4. concentrationconcentrated
  5. customRecrystallized from dichloromethane-ethanol

출처 및 근거

ORD 기록
ord-af77400b8be441a1b92213e2dd8434a2
출처 데이터셋
uspto-grants-1988_11
특허 번호
US04788130

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