Thionyl Chloride → HCID 15935408, compound
Reaction equation
[C:1]([C:9]1[CH:10]=[C:11]([CH2:15][C:16]([OH:18])=O)[CH:12]=[CH:13][CH:14]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.S(Cl)([Cl:21])=O>>[C:1]([C:9]1[CH:10]=[C:11]([CH2:15][C:16]([Cl:21])=[O:18])[CH:12]=[CH:13][CH:14]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
3
Procedure
20 g of m-benzoyl-phenyl acetic acid (prepared by process of French patent No. 1,546,478) and 100 ml of thionyl chloride were refluxed for 3 hours and then evaporated to dryness. Excess thionyl chloride was removed by entrainment with benzene to obtain 21.74 g of m-benzoyl-phenyl-acetic acid chloride.
Workup
- customevaporated to dryness
- customExcess thionyl chloride was removed by entrainment with benzene
Sources & evidence
- ORD record
- ord-3854e3179d85418f831789d4fc4577a2
- Source dataset
- uspto-grants-1976_11
- Patent number
- US03995056
Reaction notes
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