Thionyl Chloride → HCID 20343343, compound
Reaction equation
S(Cl)([Cl:3])=O.[F:5][C:6]([F:21])([F:20])[O:7][C:8]1[CH:19]=[CH:18][C:11]([CH:12](O)[C:13]([CH3:16])([CH3:15])[CH3:14])=[CH:10][CH:9]=1>>[Cl:3][CH:12]([C:11]1[CH:18]=[CH:19][C:8]([O:7][C:6]([F:21])([F:20])[F:5])=[CH:9][CH:10]=1)[C:13]([CH3:16])([CH3:15])[CH3:14]Participants
3
Procedure
To freshly distilled thionyl chloride (14.87 g, 0.125 mol) cooled in salt ice bath is added in portions the neopentyl alcohol of Example 24 (12.4 g, 0.05 mol) over 30 minutes. The ice bath is removed and the slurry is left to stand overnight. Evaporation of excess thionyl chloride gives a solid.
Workup
- customThe ice bath is removed
- waitthe slurry is left
- customEvaporation of excess thionyl chloride
- customgives a solid
Sources & evidence
- ORD record
- ord-f97e0fa9408648b6891fdb2e383aa868
- Source dataset
- uspto-grants-1979_12
- Patent number
- US04178460
Reaction notes
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