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Water → (3-Acetamidophenyl) acetate

HRID 1773553
ノート
印刷プレビュー

反応式

HRID 1773553 の反応式
[C:1]([O:4][C:5](=O)[CH3:6])(=[O:3])[CH3:2].[NH2:8][C:9]1[CH:10]=[C:11](O)C=C[CH:14]=1.[OH2:16].N1[CH:22]=[CH:21]C=CC=1>CN(C)C1C=CN=CC=1>[C:21]([NH:8][C:9]1[CH:14]=[C:5]([O:4][C:1](=[O:3])[CH3:2])[CH:6]=[CH:11][CH:10]=1)(=[O:16])[CH3:22]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 1049PyridineHCID 7918Acetic AnhydrideHCID 115683-Aminophenol

生成物 1

HCID 231988(3-Acetamidophenyl) acetate

試薬・触媒・溶媒 1

HCID 142844-(Dimethylamino)pyridine触媒

実験手順

Acetic anhydride (53 mL, 572.0 mmol) was slowly added to a mixture of 3-aminophenol (25 g, 225.0 mmol) and 4-dimethylaminopyridine (catalytic quantity) in pyridine (100 mL) at 0° C. and the reaction mixture was stirred at room temperature for 62 hours. Water (1 L) was added and the resulting mixture was extracted with ethyl acetate. The organic extracts were washed with an aqueous solution of hydrochloric acid, a saturated aqueous solution of sodium bicarbonate and water, dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure to give 21.79 g of acetic acid 3-acetylamino-phenyl ester as a solid without further purifications. A second batch (2.978 g) of this material crashed out of the aqueous layer upon standing and was collected by filtration.

後処理

  1. extractionthe resulting mixture was extracted with ethyl acetate
  2. washThe organic extracts were washed with an aqueous solution of hydrochloric acid
  3. dry with materiala saturated aqueous solution of sodium bicarbonate and water, dried over anhydrous sodium sulfate
  4. filtrationfiltered
  5. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-e769f0f6c7d445658f464a969613e7fc
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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