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Potassium Carbonate → Acetamide, N-(3-hydroxy-4-nitrophenyl)-

HRID 1773555
ノート
印刷プレビュー

反応式

HRID 1773555 の反応式
[C:1]([NH:4][C:5]1[CH:6]=[CH:7][C:8]([N+:15]([O-:17])=[O:16])=[C:9]([O:11]C(=O)C)[CH:10]=1)(=[O:3])[CH3:2].C(=O)([O-])[O-].[K+].[K+]>CO>[OH:11][C:9]1[CH:10]=[C:5]([NH:4][C:1](=[O:3])[CH3:2])[CH:6]=[CH:7][C:8]=1[N+:15]([O-:17])=[O:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 11430Potassium CarbonateHCID 127921275-Acetamido-2-nitrophenyl acetate

生成物 1

HCID 10176525Acetamide, N-(3-hydroxy-4-nitrophenyl)-

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A mixture of acetic acid 5-acetylamino-2-nitro-phenyl ester (20.5 g, 85.77 mmol) and potassium carbonate (26 g, 188.4 mmol) in methanol (200 mL) was stirred at room temperature for 3 hours. The reaction mixture was concentrated under reduced pressure, water (250 mL) was added and the resulting mixture was acidified by addition of concentrated hydrochloric acid. The solid which crushed out was triturated, collected by filtration, washed with water and dried under vacuum to afford N-(3-hydroxy-4-nitro-phenyl)-acetamide.

後処理

  1. concentrationThe reaction mixture was concentrated under reduced pressure, water (250 mL)
  2. additionwas added
  3. additionthe resulting mixture was acidified by addition of concentrated hydrochloric acid
  4. customThe solid which crushed out
  5. customwas triturated
  6. filtrationcollected by filtration
  7. washwashed with water
  8. customdried under vacuum

出典と根拠

ORDレコード
ord-d5291b0c53284b099630f211e21abe93
出典データセット
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09255110B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート