Water → (7-Dipropylamino-5,6,7,8-tetrahydro-naphthalen-1-yl)-methanol

HRID 274805노트

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HRID 274805 반응식
[CH2:1]([N:4]([CH2:19][CH2:20][CH3:21])[CH:5]1[CH2:14][CH2:13][C:12]2[C:7](=[C:8]([C:15](OC)=[O:16])[CH:9]=[CH:10][CH:11]=2)[CH2:6]1)[CH2:2][CH3:3].[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[OH-].[Na+]>O1CCCC1>[CH2:19]([N:4]([CH2:1][CH2:2][CH3:3])[CH:5]1[CH2:14][CH2:13][C:12]2[C:7](=[C:8]([CH2:15][OH:16])[CH:9]=[CH:10][CH:11]=2)[CH2:6]1)[CH2:20][CH3:21]

참가 물질

6

실험 절차

Alternatively,a solution of 2-dipropylamino-8-methoxycarbonyl-1,2,3,4-tetrahydronaphthalene (480 mg, 1.66 mMol) in tetrahydrofuran (5 mL) was added dropwise to a suspension of lithium aluminum hydride (100 mg, 2.49 mMol) in tetrahydrofuran (10 mL), and the reaction mixture was stirred at room temperature for 2.5 hours. The reaction mixture was then cooled to 0° C., and to it were added sequentially water (0.1 mL), 15% aqueous sodium hydroxide (0.1 mL) and water (0.3 mL). The suspension was then stirred at room temperature for one-half hour and was then filtered through a bed of Celite. The filtrate was concentrated in vacuo to give the title compound as a colorless, viscous oil (400 mg, 92%). The hydrochloride salt was formed and recrystallized (ethanol/diethyl ether) to give colorless crystals (m.p.=142° C.). Analysis: Calculated for C17H27NO·HCl: Theory: C, 69.02, H, 8.86, N, 4.73; Found: C, 69.03, H, 8.72, N, 4.61.

후처리

  1. temperatureThe reaction mixture was then cooled to 0° C.
  2. stirringThe suspension was then stirred at room temperature for one-half hour
  3. filtrationwas then filtered through a bed of Celite
  4. concentrationThe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-67a6abff10f5454d9ae3aa4feabdb58b
출처 데이터셋
uspto-grants-1995_02
특허 번호
US05389687

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