Thionyl Chloride →
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([C:9]2([CH:16]([CH3:18])[CH3:17])[O:15][CH2:14][O:13]O[C:10]2=[O:11])[CH:5]=[CH:6][C:7]=1[F:8].S(Cl)([Cl:21])=O>>[F:1][C:2]1[CH:3]=[C:4]([C:9]2([CH:16]([CH3:18])[CH3:17])[O:15][CH2:14][O:13][ClH:21][C:10]2=[O:11])[CH:5]=[CH:6][C:7]=1[F:8]Participants
2
Reactant 2
Product 0
No Product data yet.
Procedure
30 g of 3,4-difluoromethylenedioxy-α-isopropylphenylacetic acid were dissolved in 150 ml of thionyl chloride and the solution was heated to the boil for 1 hour. After distilling off excess thionyl chloride, the residue was distilled under a high vacuum. 3,4-Difluoromethylenedioxy-α-isopropyl-phenylacetic acid chloride of boiling point 83°-86° C./0.3 mm Hg was obtained.
Workup
- temperaturethe solution was heated to the boil for 1 hour
- distillationAfter distilling off excess thionyl chloride
- distillationthe residue was distilled under a high vacuum
Sources & evidence
- ORD record
- ord-ae39e9163c12492f8b0ae529197b7d61
- Source dataset
- uspto-grants-1981_08
- Patent number
- US04284643
Reaction notes
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