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Sodium Hydroxide → HCID 23288445, 화합물

HRID 368384
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HRID 368384 반응식
[OH:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[NH:11][C:12]([NH:14][CH:15]([C:19](OCC)=[O:20])[CH:16]([CH3:18])[CH3:17])=[O:13].[OH-].[Na+]>C(O)C.O>[OH:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[NH:11][C:12]([NH:14][C:15](=[C:19]=[O:20])[CH:16]([CH3:18])[CH3:17])=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 23288448HCID 23288448, 화합물

생성물 1

HCID 23288445HCID 23288445, 화합물수율 49.7%

시약·촉매·용매 1

HCID 19096565Water ethanol용매

실험 절차

To a solution of N-(2-Hydroxy-4-nitrophenyl)-N'-[1-(ethoxycarbonyl)-2-methylpropyl)urea (200 mg, 0.62 mmol) in ethanol/water (10 mL/1 mL), sodium hydroxide (123 mg, 3.1 mmol) was added. The reaction mixture was stirred at reflux temperature for 16 hours. Then the reaction mixture was cooled to room temperature and all the solvent was evaporated. 3N of HCl was added to pH=1. A yellow solid precipitated, it was filtered to give desired product (86 mg, 47%). EI-MS m/z 298.3 (M+). mp: 168.4-169.2° C.

후처리

  1. temperatureat reflux temperature for 16 hours
  2. customall the solvent was evaporated
  3. addition3N of HCl was added to pH=1
  4. customA yellow solid precipitated
  5. filtrationit was filtered

출처 및 근거

ORD 기록
ord-eed21f7246bf4fa088907b4d7dfea8bc
출처 데이터셋
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06133319

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