Thionyl Chloride → HCID 20448118, compound
Reaction equation
O[C:2]1[C:3](O)=[CH:4][C:5]2[S:10][CH:9]=[C:8]([C:11](O)=[O:12])[C:7](=[O:14])[C:6]=2[CH:15]=1.S(Cl)([Cl:19])=O>>[O:14]=[C:7]1[C:6]2=[CH:15][CH2:2][CH2:3][CH:4]=[C:5]2[S:10][CH:9]=[C:8]1[C:11]([Cl:19])=[O:12]Participants
3
Procedure
6,7-Dihydroxy-4-oxo-4H-1-benzothiopyran-3-carboxylic acid (100 mg) was heated under reflux for 2 hours in thionyl chloride (5 mL), and then the thionyl chloride was distilled off. To the residue was added benzene (20 mL). Benzene was distilled off again and the residue was vacuum dried to give 6,7-dihydro-4-oxo-4H-1-benzothiopyran-3-carbonyl chloride.
Workup
- distillationthe thionyl chloride was distilled off
- additionTo the residue was added benzene (20 mL)
- distillationBenzene was distilled off again
- customdried
Sources & evidence
- ORD record
- ord-2404f10bfdb34dd4942e222d4324e37a
- Source dataset
- uspto-grants-1984_08
- Patent number
- US04468394
Reaction notes
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