Hydrochloric Acid → p-{[2-(2-Naphthyloxy)ethyl]amino}benzoic acid
反応式
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[O:11][CH2:12][CH2:13][NH:14][C:15]1[CH:25]=[CH:24][C:18]([C:19]([O:21]CC)=[O:20])=[CH:17][CH:16]=1.[OH-].[K+].Cl>C(O)C.O.O>[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[O:11][CH2:12][CH2:13][NH:14][C:15]1[CH:25]=[CH:24][C:18]([C:19]([OH:21])=[O:20])=[CH:17][CH:16]=1参加物
6
実験手順
A mixture of 3.0 g of ethyl p-{[2-(2-naphthyloxy)-ethyl]amino}benzoate, and 3.0 g of potassium hydroxide in 200 ml of ethanol-water (95:5) is refluxed for 3 hours. The mixture is diluted with 100 ml of water and brought to pH 6.0 with concentrated hydrochloric acid. The mixture is filtered and the solid washed with 50 ml of water and 20 ml of cold ethanol-water (4:1) to give the product, mp 208°-211° C.
後処理
- temperatureis refluxed for 3 hours
- filtrationThe mixture is filtered
- washthe solid washed with 50 ml of water and 20 ml of cold ethanol-water (4:1)
- customto give the product, mp 208°-211° C.
出典と根拠
- ORDレコード
- ord-f6ebdbaed33e415fbc59f1491b6d7e68
- 出典データセット
- uspto-grants-1980_01
- 特許番号
- US04182776
反応ノート
読み込み中…