Hydrochloric Acid → HCID 70456365, compound
Reaction equation
C([O:3][C:4]([C:6]1[CH:21]=[CH:20][C:9]2[S:10][C:11]([CH2:14][C:15]3[NH:16][CH:17]=[CH:18][N:19]=3)=[C:12]([CH3:13])[C:8]=2[CH:7]=1)=[O:5])C.[ClH:22]>>[ClH:22].[NH:19]1[CH:18]=[CH:17][N:16]=[C:15]1[CH2:14][C:11]1[S:10][C:9]2[CH:20]=[CH:21][C:6]([C:4]([OH:5])=[O:3])=[CH:7][C:8]=2[C:12]=1[CH3:13]Participants
3
Procedure
A mixture of 2-(1-imidazolylmethyl)-3-methylbenzo[b]thiophene-5-carboxylic acid ethyl ester (1.0 g) and 6N hydrochloric acid (80 ml) was heated on a steam bath for 5 hours and then cooled. The solid was filtered off, dried and crystallized from ethanol ether to give 2-(1-imidazolylmethyl)-3-methylbenzo[b]thiophene-5-carboxylic acid hydrochloride (0.72 g), m.p. 298°-299° C.
Workup
- temperaturewas heated on a steam bath for 5 hours
- temperaturecooled
- filtrationThe solid was filtered off
- customdried
- customcrystallized from ethanol ether
Sources & evidence
- ORD record
- ord-b2533cc39e37411983a058687e1e4522
- Source dataset
- uspto-grants-1986_05
- Patent number
- US04590200
Reaction notes
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