Thionyl Chloride → HCID 20225301, compound
Reaction equation
[CH3:1][O:2][CH:3](OC)[CH2:4][O:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.S(Cl)([Cl:16])=O>C(Cl)(=O)C>[Cl:16][CH:3]([O:2][CH3:1])[CH2:4][O:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To 36 g of phenoxyacetaldehyde dimethyl acetal was added, dropwise, 40 ml of acetyl chloride and 0.5 ml of thionyl chloride. After 15 h at room temperature the solution was evaporated and the residue distilled under vacuum, 110°-120° C./1 mm, to yield the title compound as a colourless oil.
Workup
- customAfter 15 h at room temperature the solution was evaporated
- distillationthe residue distilled under vacuum, 110°-120° C./1 mm
Sources & evidence
- ORD record
- ord-c44db6b523f647cc896b886c7d59af07
- Source dataset
- uspto-grants-1986_12
- Patent number
- US04629737
Reaction notes
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