Thionyl Chloride → 3-(3'-p-Chlorobenzoyl-phenyl)-propionyl chloride
Reaction equation
[Cl:1][C:2]1[CH:20]=[CH:19][C:5]([C:6]([C:8]2[CH:9]=[C:10]([CH2:14][CH2:15][C:16](O)=[O:17])[CH:11]=[CH:12][CH:13]=2)=[O:7])=[CH:4][CH:3]=1.S(Cl)([Cl:23])=O>>[Cl:1][C:2]1[CH:20]=[CH:19][C:5]([C:6]([C:8]2[CH:9]=[C:10]([CH2:14][CH2:15][C:16]([Cl:23])=[O:17])[CH:11]=[CH:12][CH:13]=2)=[O:7])=[CH:4][CH:3]=1Participants
3
Procedure
6.96 g of 3-(3'-p-chlorobenzoyl-phenyl)-propionic acid and 70 ml of thionyl chloride were refluxed for 3 hours and then evaporated to dryness. The residue was taken up in 100 ml of benzene and evaporated to dryness to obtain 8.7 g of 3-(3'-p-chlorobenzoyl-phenyl)-propionyl chloride which was used as is.
Workup
- customevaporated to dryness
- customevaporated to dryness
Sources & evidence
- ORD record
- ord-9ce98d955ee84fe4bb63bcc3f94edb73
- Source dataset
- uspto-grants-1976_01
- Patent number
- US03931302
Reaction notes
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