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Sodium Hydroxide → HCID 53898632, 화합물

HRID 263464
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HRID 263464 반응식
[C:1]12([NH:11][C:12](=[O:28])[CH:13]=[CH:14][C:15]3[CH:20]=[CH:19][C:18]([O:21]C(=O)C)=[C:17]([N+:25]([O-:27])=[O:26])[CH:16]=3)[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH2:2]1)[CH2:8]2.[OH-].[Na+]>CO>[C:1]12([NH:11][C:12](=[O:28])[CH:13]=[CH:14][C:15]3[CH:20]=[CH:19][C:18]([OH:21])=[C:17]([N+:25]([O-:27])=[O:26])[CH:16]=3)[CH2:10][CH:5]3[CH2:4][CH:3]([CH2:9][CH:7]([CH2:6]3)[CH2:8]1)[CH2:2]2
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 53874822N-(1-Adamantyl)-4-acetoxy-3-nitrocinnamamide

생성물 1

HCID 53898632HCID 53898632, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

1 g of N-(1-adamantyl)-4-acetoxy-3-nitrocinnamamide (prepared as described in Example 1) was dissolved in 30 ml of methanol; 30 ml of a 4N aqueous solution of sodium hydroxide were then added, and the resulting mixture was stirred for 3 hours at room temperature. At the end of this time, the methanol was removed by distillation under reduced pressure. Addition of 3N aqueous hydrochloric acid to the residue afforded crystals of the title compound, melting at 162°-163° C.

후처리

  1. customAt the end of this time, the methanol was removed by distillation under reduced pressure
  2. additionAddition of 3N aqueous hydrochloric acid to the residue

출처 및 근거

ORD 기록
ord-a20e237348b5499ab64cb91c3f4fabc5
출처 데이터셋
uspto-grants-1997_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05643925

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