Thionyl Chloride → HCID 19972568, compound
Reaction equation
O[CH2:2][CH2:3][O:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[S:11][CH3:12].S(Cl)([Cl:15])=O>>[Cl:15][CH2:2][CH2:3][O:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[S:11][CH3:12]Participants
3
Procedure
o-(β-Hydroxyethoxy)-thioanisole (0.1 mole) is refluxed in excess thionyl chloride and evaporated to dryness to yield o-(β-chloroethoxy)-thioanisole.
Workup
- customevaporated to dryness
Sources & evidence
- ORD record
- ord-43f3c1c561d040579f5f65e63a4f5f8f
- Source dataset
- uspto-grants-1976_01
- Patent number
- US03932498
Reaction notes
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