Thionyl Chloride → 7,8-Dihydroxychromone-3-carbonyl chloride
Reaction equation
[OH:1][C:2]1[C:11]([OH:12])=[C:10]2[C:5]([C:6](=[O:16])[C:7]([C:13](O)=[O:14])=[CH:8][O:9]2)=[CH:4][CH:3]=1.S(Cl)([Cl:19])=O>>[OH:1][C:2]1[C:11]([OH:12])=[C:10]2[C:5]([C:6](=[O:16])[C:7]([C:13]([Cl:19])=[O:14])=[CH:8][O:9]2)=[CH:4][CH:3]=1Participants
3
Procedure
A mixture of 7,8-dihydroxychromone-3-carboxylic acid (6.6 g, 30 mmol) and thionyl chloride (25 ml) was refluxed for 1 hour, and the thionyl chloride was removed. After the addition of benzene to the residue, the mixture was evaporated to dryness and the residue was triturated with n-hexane to give the desired compound (7.2 g).
Workup
- temperaturewas refluxed for 1 hour
- customthe thionyl chloride was removed
- additionAfter the addition of benzene to the residue
- customthe mixture was evaporated to dryness
- customthe residue was triturated with n-hexane
Sources & evidence
- ORD record
- ord-bcce56a5346842ba957b65853933add9
- Source dataset
- uspto-grants-1981_08
- Patent number
- US04285940
Reaction notes
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