Hydrochloric Acid → 2,4-Diaminophenyl beta-hydroxypropyl ether dihydrochloride
反応式
[ClH:1].[OH:2][CH:3]([CH3:17])[CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([NH2:12])=[CH:8][C:7]=1[NH:13]C(=O)C.Cl>C(O)C>[ClH:1].[ClH:1].[OH:2][CH:3]([CH3:17])[CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([NH2:12])=[CH:8][C:7]=1[NH2:13]参加物
4
実験手順
0.109 mol (28.4 g) of 2-acetylamino-4-aminophenyl β-hydroxypropyl ether monohydrochloride is dissolved, under reflux, in a mixture of 80 ml of ethanol saturated with hydrogen chloride and 25 ml of 36% strength hydrochloric acid. The reaction mixture is heated under reflux for 11/2 hours. On cooling, the expected product precipitates in the form of the dihydrochloride. The product is filtered off, washed with a small amount of absolute alcohol and dried in vacuo at 50° C. It melts with decomposition at between 215° and 220° C.
後処理
- temperatureThe reaction mixture is heated
- temperatureunder reflux for 11/2 hours
- temperatureOn cooling
- customthe expected product precipitates in the form of the dihydrochloride
- filtrationThe product is filtered off
- washwashed with a small amount of absolute alcohol
- customdried in vacuo at 50° C
- custommelts with decomposition at between 215° and 220° C.
出典と根拠
- ORDレコード
- ord-1406f15bbb864d2e8708bdf1b449b1d1
- 出典データセット
- uspto-grants-1991_06
- 特許番号
- US05026401
反応ノート
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