Hydrochloric Acid → 2-Amino-6-trifluoromethylbenzyl chloride
Reaction equation
[NH2:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10]([F:13])([F:12])[F:11])[C:3]=1[CH2:4]O.[ClH:14]>>[NH2:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10]([F:13])([F:12])[F:11])[C:3]=1[CH2:4][Cl:14]Participants
3
Procedure
To 4.06 g (7.8 mmole) of 2-amino-6-trifluoromethylbenzyl alcohol in a pressure bottle was added 60 ml of concentrated hydrochloric acid, the bottled stoppered and immersed in an oil bath maintained at 100°. The mixture was stirred for 1.5 hr., cooled and the precipitate filtered under suction. The colorless solid was washed with water and dried under high vacuum, yielding 3.28 g (75% yield) of a colorless solid; mp 155°-161°. The sample was used as such without further purification.
Workup
- customimmersed in an oil bath
- temperaturemaintained at 100°
- temperature, cooled
- filtrationthe precipitate filtered under suction
- washThe colorless solid was washed with water
- customdried under high vacuum
Sources & evidence
- ORD record
- ord-60e0efe7ac2948af85ab7841257830d6
- Source dataset
- uspto-grants-1984_06
- Patent number
- USRE031617
Reaction notes
Loading…