Hydrochloric Acid → HCID 20377674, compound
Reaction equation
C[O:2][C:3]([C:5]1[S:9][C:8]2[S:10][C:11]([C:13]([C:15]3[CH:16]=[C:17]([CH:21]([CH3:26])[C:22]([O:24]C)=[O:23])[CH:18]=[CH:19][CH:20]=3)=[O:14])=[CH:12][C:7]=2[CH:6]=1)=[O:4].Cl>[OH-].[K+]>[C:3]([C:5]1[S:9][C:8]2[S:10][C:11]([C:13]([C:15]3[CH:16]=[C:17]([CH:21]([CH3:26])[C:22]([OH:24])=[O:23])[CH:18]=[CH:19][CH:20]=3)=[O:14])=[CH:12][C:7]=2[CH:6]=1)([OH:4])=[O:2]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 20 °C
Procedure
Methyl 2-{3-(5-methoxycarbonyl-thieno[2,3-b]thien-2-yl)carbonyl-phenyl}propionate (36 g) in solution in a mixture of potassium hydroxide pellets (26.4 g), distilled water (160 cc) and ethanol (400 cc), is stirred for 17 hours at a temperature of about 20° C. The resulting suspension is diluted with distilled water (800 cc) and filtered. The filtrate is stirred with decolourizing charcoal (3 g) and filtered. The solution obtained is added dropwise to a 5 N aqueous solution of hydrogen chloride (400 cc) cooled in an ice bath, the rate of addition being regulated in such a way that the temperature of the mixture remains below 10° C. The reaction mixture is stirred for a further hour in the ice bath, and then the resulting crystals are filtered off, washed three times with distilled water (total 150 cc), and dried in air. Crude 2-{3-(5-carboxy-thieno[2,3-b]thien-2-yl)carbonylphenyl}propionic acid (24.3 g), melting at 244° C., is thus obtained.
Workup
- distillationdistilled water (160 cc) and ethanol (400 cc)
- additionThe resulting suspension is diluted with distilled water (800 cc)
- filtrationfiltered
- stirringThe filtrate is stirred with decolourizing charcoal (3 g)
- filtrationfiltered
- customThe solution obtained
- temperaturecooled in an ice bath
- additionthe rate of addition
- customremains below 10° C
- filtrationthe resulting crystals are filtered off
- washwashed three times with distilled water (total 150 cc)
- customdried in air
Sources & evidence
- ORD record
- ord-8c8a230bbb21444f8795e0c72bbcfab6
- Source dataset
- uspto-grants-1980_01
- Patent number
- US04183944
Reaction notes
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