Hydrochloric Acid → 4-(methoxycarbonyl)-2-methylthiophen-3-aminium chloride
Reaction equation
[C:1]([CH:5]1[CH2:9][S:8][CH:7]([CH3:10])[C:6]1=[N:11]O)([O:3][CH3:4])=[O:2].[ClH:13]>CCOCC>[ClH:13].[NH2:11][C:6]1[C:5]([C:1]([O:3][CH3:4])=[O:2])=[CH:9][S:8][C:7]=1[CH3:10]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 41.1 g. (0.217 mole) of 4-carbomethoxy-3-keto-2-methyltetrahydrothiophene oxime in 600 ml. anhydrous ether, previously saturated with gaseous hydrogen chloride at 0°, was allowed to stir at 25° overnight. The separated solid was collected, washed well with ether, and dried to afford 33.2 g. Evaporation of the filtrate yielded after recrystallization of the residue an additional 4.2 g. to afford a total yield of pure 3-amino-4-carbomethoxy-2-methylthiophene hydrochloride of 37.4 g. (84%). The compound melts 191°-192°.
Workup
- customat 0°
- customThe separated solid was collected
- washwashed well with ether
- customdried
- customto afford 33.2 g
- customEvaporation of the filtrate
- customyielded
- customafter recrystallization of the residue an additional 4.2 g
Sources & evidence
- ORD record
- ord-9652d91d96be4c459bbedeb41837406c
- Source dataset
- uspto-grants-1982_03
- Patent number
- US04317915
Reaction notes
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