Benzocaine → 4-(Methylsulfonamido)benzoic acid
反応式
[NH2:1][C:2]1[CH:12]=[CH:11][C:5]([C:6]([O:8]CC)=[O:7])=[CH:4][CH:3]=1.CCN(CC)CC.[CH3:20][S:21](Cl)(=[O:23])=[O:22]>C(Cl)Cl.O>[CH3:20][S:21]([NH:1][C:2]1[CH:12]=[CH:11][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=1)(=[O:23])=[O:22]参加物
反応条件
- 温度
- 0 °C
実験手順
Ethyl 4-amino-benzoate (5 g, 30 mmol, 1.0 equiv) was mixed in 50 mL of CH2Cl2 with Et3N (6.1 g, 60 mmol, 2.0 equiv). The solution was cooled to 0° C. and methanesulfonyl chloride (3.8 g, 33 mmol. 1.1 equiv) was added as a solution in 15 mL of CH2Cl2 dropwise over a 15 min period. The reaction was stirred for 4 h at which time it was diluted with 50 mL of water. Layers were separated and the organic layer was washed with 50 mL of saturated sodium bicarbonate solution and concentrated. The resulting ester was dissolved in 50 mL of MeOH and treated with 50 mL of 5 N NaOH for 4 h. The reaction solution was extracted with Et2O and the aqueous layer was acidified to give a white precipitate that was collected by filtration. The solid was dried and used without further purification.
後処理
- customLayers were separated
- washthe organic layer was washed with 50 mL of saturated sodium bicarbonate solution
- concentrationconcentrated
- dissolutionThe resulting ester was dissolved in 50 mL of MeOH
- additiontreated with 50 mL of 5 N NaOH for 4 h
- extractionThe reaction solution was extracted with Et2O
- customto give a white precipitate that
- filtrationwas collected by filtration
- customThe solid was dried
- customused without further purification
出典と根拠
- ORDレコード
- ord-24d1b58da3704a99a5c164dd93147823
- 出典データセット
- uspto-grants-2004_06
- 特許番号
- US06756372B2
反応ノート
読み込み中…