Phosphorus oxychloride → Ethyl 4-(chlorosulfonyl)benzoate

HRID 1829853

反応式

HRID 1829853 の反応式
[CH2:1]([O:3][C:4]([C:6]1[CH:11]=[CH:10][C:9]([S:12]([O-:15])(=O)=[O:13])=[CH:8][CH:7]=1)=[O:5])[CH3:2].[K+].O=P(Cl)(Cl)[Cl:19]>C(#N)C.S1(CCCC1)(=O)=O>[CH2:1]([O:3][C:4]([C:6]1[CH:11]=[CH:10][C:9]([S:12]([Cl:19])(=[O:15])=[O:13])=[CH:8][CH:7]=1)=[O:5])[CH3:2]

参加物

5

反応条件

温度
75 °C

実験手順

A round bottom flask, fitted with a magnetic stir bar and a hose adapter connected to a source of nitrogen gas, was charged with a solution of potassium 4-ethoxycarbonylbenzenesulfonate (75.1 g) dissolved in a 3:1 (v/v) mixture of acetonitrile (300 mL) and sulfolane (100 mL). As the solution was stirred, POCl3 (55 mL) was added slowly and the stirring mixture was heated at 75° C. under a nitrogen atmosphere for 3 hours. The heterogeneous reaction mixture was allowed to cool to room temperature and was then concentrated using a rotary evaporator. The flask was then cooled in an ice bath and ice was added to the mixture in the flask. The product crystallized as a white solid and was filtered and washed with cold deionized water. The product was dried under vacuum at room temperature and 3 mmHg for 2 hours to afford 76 g of white solid.

後処理

  1. customA round bottom flask, fitted with a magnetic stir bar and a hose adapter
  2. temperatureto cool to room temperature
  3. concentrationwas then concentrated
  4. customa rotary evaporator
  5. temperatureThe flask was then cooled in an ice bath
  6. additionice was added to the mixture in the flask
  7. customThe product crystallized as a white solid
  8. filtrationwas filtered
  9. washwashed
  10. customThe product was dried under vacuum at room temperature

出典と根拠

ORDレコード
ord-7619f34fe18645bd8c42e2f7a8c4e95f
出典データセット
uspto-grants-2006_06
特許番号
US07064152B2

関連ノート

読み込み中…