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Sodium Hydroxide → 4-Neopentyl-2-nitroaniline

HRID 1424227
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인쇄 미리보기

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HRID 1424227 반응식
[CH2:1]([C:6]1[CH:11]=[CH:10][C:9]([NH:12]C(=O)C)=[C:8]([N+:16]([O-:18])=[O:17])[CH:7]=1)[C:2]([CH3:5])([CH3:4])[CH3:3].[OH-].[Na+]>O>[CH2:1]([C:6]1[CH:11]=[CH:10][C:9]([NH2:12])=[C:8]([N+:16]([O-:18])=[O:17])[CH:7]=1)[C:2]([CH3:5])([CH3:4])[CH3:3]
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 85802767N-(4-Neopentyl-2-nitrophenyl)acetamide

생성물 1

HCID 858027694-Neopentyl-2-nitroaniline수율 90%

시약·촉매·용매 1

HCID 962Water용매

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온도
90 °C

실험 절차

A suspension of N-(4-neopentyl-2-nitrophenyl)acetamide (Preparation 87, 3.0 g, 12.0 mmol) in aqueous sodium hydroxide (6.0 M, 20 mL, 120 mmol) was heated at 90° C. for 36 hours. After cooling, a small amount of water was added and the mixture extracted with dichloromethane (5×). The organic layers were combined, dried over anhydrous magnesium sulphate, filtered, and concentrated in vacuo to provide the title compound (2.15 g, 90%) as a yellow solid.

후처리

  1. temperatureAfter cooling
  2. extractionthe mixture extracted with dichloromethane (5×)
  3. dry with materialdried over anhydrous magnesium sulphate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-5f4e2452d9f24f978c3e2aaab21f9e55
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08927587B2

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