Water → HCID 178492972, compound
Reaction equation
[CH3:1][O:2][C:3]1[C:4]([C:9]([OH:11])=[S:10])=[C:5]([CH3:8])[S:6][CH:7]=1.[Cl:12]N1C(=O)CCC1=O.O>C(Cl)(Cl)Cl.C(O)(=O)C>[Cl:12][C:7]1[S:6][C:5]([CH3:8])=[C:4]([C:9]([OH:11])=[S:10])[C:3]=1[O:2][CH3:1]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Equimolecular amounts of the thiophene (d) above and N-chlorosuccinimide were dissolved in 1/1 chloroform/acetic acid mixture. The mixture was stirred for two hours and then poured into water. The organic layer was washed with 10% aqueous sodium hydroxide, dried over sodium sulphate and the solvent evaporated. The carboxylic acid was purified by recrystallisation from ethanol, m.p. 193°-194° C.
Workup
- washThe organic layer was washed with 10% aqueous sodium hydroxide
- dry with materialdried over sodium sulphate
- customthe solvent evaporated
- customThe carboxylic acid was purified by recrystallisation from ethanol, m.p. 193°-194° C.
Sources & evidence
- ORD record
- ord-93487e119c8f482eadf6a1943ec07b9f
- Source dataset
- uspto-grants-1991_05
- Patent number
- US05015656
Reaction notes
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