Acetic Anhydride → HCID 67958188、化合物

HRID 527544

反応式

HRID 527544 の反応式
[Br:1][C:2]1[C:7]([OH:8])=[CH:6][CH:5]=[CH:4][C:3]=1[OH:9].[C:10](OC(=O)C)(=[O:12])[CH3:11]>ClCCl>[C:10]([O:9][C:3]1[CH:4]=[CH:5][CH:6]=[C:7]([OH:8])[C:2]=1[Br:1])(=[O:12])[CH3:11]

参加物

4

実験手順

To a solution of 2-bromo-1,3-benzenediol (3.028 g, 16.02 mmol) in dichloromethane (70 ml), TEA (3.35 ml, 24.03 mmol) and acetic anhydride (1.512 ml, 16.02 mmol) were added under stirring. The reaction mixture was stirred at room temperature overnight. The reaction was quenched with a saturated solution of ammonium chloride (100 ml), and extracted with ethyl acetate (3 times 70 ml). The combined organic layers were dried over sodium sulphate, filtered and evaporated to afford the title compound as a black oil which was used directly used in the next step. (3.028 g)

後処理

  1. stirringThe reaction mixture was stirred at room temperature overnight
  2. customThe reaction was quenched with a saturated solution of ammonium chloride (100 ml)
  3. extractionextracted with ethyl acetate (3 times 70 ml)
  4. dry with materialThe combined organic layers were dried over sodium sulphate
  5. filtrationfiltered
  6. customevaporated

出典と根拠

ORDレコード
ord-1817205af72a44ac9f44e75cec3b4ab0
出典データセット
uspto-grants-2016_05
特許番号
US09346790B2

関連ノート

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