Hydrochloric Acid → HCID 13472266, compound
Reaction equation
[N+:1]([C:4]1[C:12]2[CH2:11][S:10][C:9](=[O:13])[C:8]=2[CH:7]=[CH:6][CH:5]=1)([O-])=O.[ClH:14]>>[ClH:14].[O:13]=[C:9]1[C:8]2[CH:7]=[CH:6][CH:5]=[C:4]([NH2:1])[C:12]=2[CH2:11][S:10]1Participants
3
Procedure
4-Nitrobenzo[c]thiophene-1(3H)-one (38.1 g) was added portionwise to a solution of 146.0 g of stannous chloride dihydrate in 325 ml concentrated hydrochloric acid. A slow exotherm from 18° to 42° occurred and the reaction mixture was maintained at 40°-45° by cooling. When the exotherm subsided, the suspension was stirred while cooling to ambient temperature (3.5 hours). The solid was collected, washed with a small volume of cold concentrated hydrochloric acid, then dried under nitrogen to give 57.7 g of crude 1,3-dihydro-1-oxobenzo[c]thiophene-4-amine hydrochloride, m.p. 205°(d).
Workup
- customfrom 18° to 42°
- temperaturethe reaction mixture was maintained at 40°-45°
- temperatureby cooling
- customThe solid was collected
- washwashed with a small volume of cold concentrated hydrochloric acid
- customdried under nitrogen
Sources & evidence
- ORD record
- ord-05a324f4402741408c24e634cccd45e7
- Source dataset
- uspto-grants-1987_08
- Patent number
- US04687508
Reaction notes
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