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Hydrochloric Acid → 1-Acetyl-7-hydroxy-2,3,4,5-tetrahydro-1H-benzazepine

HRID 1741044
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인쇄 미리보기

반응식

HRID 1741044 반응식
C([O:4][C:5]1[CH:6]=[CH:7][C:8]2[N:14]([C:15](=[O:17])[CH3:16])[CH2:13][CH2:12][CH2:11][CH2:10][C:9]=2[CH:18]=1)(=O)C.[OH-].[Na+].Cl>C(O)C.O>[C:15]([N:14]1[C:8]2[CH:7]=[CH:6][C:5]([OH:4])=[CH:18][C:9]=2[CH2:10][CH2:11][CH2:12][CH2:13]1)(=[O:17])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 218337947-Acetoxy-1-acetyl-2,3,4,5-tetrahydro-1H-benzazepine

생성물 1

HCID 218338251-Acetyl-7-hydroxy-2,3,4,5-tetrahydro-1H-benzazepine수율 63%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매2회

실험 절차

7-Acetoxy-1-acetyl-2,3,4,5-tetrahydro-1H-benzazepine (D23, 3.88 g, 16 mmol) was stirred in ethanol (40 ml) as NaOH (1.26 g, 32 mmol) was added in water (5 ml). After stirring for 30 min, the mixture was diluted with water (500 ml), and acidified with 5M HCl. The tan precipitate was filtered off and dried, yielding 2.02 g (63%) of the title compound. A further 0.80 g (25%) of this material was isolated by dichloromethane extraction of the filtrate.

후처리

  1. filtrationThe tan precipitate was filtered off
  2. customdried

출처 및 근거

ORD 기록
ord-b8ad193304a448c9b19819e47a0f6ce6
출처 데이터셋
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05972951

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