Thionyl Chloride → 6,7-Dihydroxy-4-oxo-4H-1-benzopyran-3-carbonyl chloride
Reaction equation
[OH:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[OH:12])[O:8][CH:7]=[C:6]([C:13](O)=[O:14])[C:5]2=[O:16].S(Cl)([Cl:19])=O>>[OH:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[OH:12])[O:8][CH:7]=[C:6]([C:13]([Cl:19])=[O:14])[C:5]2=[O:16]Participants
3
Procedure
A mixture of 6,7-dihydroxychromone-3-carboxylic acid (888 mg, 4 mmol) and thionyl chloride (25 ml) was refluxed for one hour and the thionyl chloride was evaporated. After the addition of benzene, the mixture was evaporated again to dryness and the residue was triturated with dichloromethane to give the desired compound (719 mg).
Workup
- temperaturewas refluxed for one hour
- customthe thionyl chloride was evaporated
- additionAfter the addition of benzene
- customthe mixture was evaporated again to dryness
- customthe residue was triturated with dichloromethane
Sources & evidence
- ORD record
- ord-94016eef1a974e3db1fd86761d3233ff
- Source dataset
- uspto-grants-1981_08
- Patent number
- US04285941
Reaction notes
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