Thionyl Chloride → HCID 14751482, compound
Reaction equation
[CH:1]([C:5]1[C:10]([O:11][CH2:12][C:13](O)=[O:14])=[C:9]([Cl:16])[CH:8]=[C:7]([Cl:17])[CH:6]=1)([CH2:3][CH3:4])[CH3:2].S(Cl)([Cl:20])=O>>[CH:1]([C:5]1[C:10]([O:11][CH2:12][C:13]([Cl:20])=[O:14])=[C:9]([Cl:16])[CH:8]=[C:7]([Cl:17])[CH:6]=1)([CH2:3][CH3:4])[CH3:2]Participants
3
Procedure
A mixture of 5.8 g of the product of Step C and 40 ml of thionyl chloride was refluxed for 2 hours and was evaporated to dryness under reduced pressure. The oil residue was washed with benzene and evaporated to dryness under reduced pressure to obtain 6.2 g of the desired product which was used as is for the next step.
Workup
- temperaturewas refluxed for 2 hours
- customwas evaporated to dryness under reduced pressure
- washThe oil residue was washed with benzene
- customevaporated to dryness under reduced pressure
Sources & evidence
- ORD record
- ord-9feeff11c4c448beb85e0d87e84673c0
- Source dataset
- uspto-grants-1991_11
- Patent number
- US05064861
Reaction notes
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