Methanol → 2,2,3-Trifluoro-3-(heptafluoropropoxy)propan-1-ol
Reaction equation
[C:1]([O:11][C:12](=[C:14]([F:16])[F:15])[F:13])([C:4]([C:7]([F:10])([F:9])[F:8])([F:6])[F:5])([F:3])[F:2].CO.[C:19]([O:24]OC(=O)C1C=CC=CC=1)(CC)(C)C>>[C:1]([O:11][CH:12]([C:14]([CH2:19][OH:24])([F:15])[F:16])[F:13])([C:4]([C:7]([F:10])([F:9])[F:8])([F:6])[F:5])([F:3])[F:2]Participants
4
Procedure
C3F7OCFHCF2CH2OH was prepared by the reaction of C3F7OCF═CF2 (53 g, 0.2 mol) with methanol (63.7 g, 2.0 mol) using t-amylperoxybenzoate (1.0 g) as free radical initiator at 106° C. The product reaction mixture was washed with water and distilled and the distillation fraction of b.r.=115-117° C. used in the next step.
Workup
- customat 106° C
- customThe product reaction mixture
- washwas washed with water
- distillationdistilled
- custom=115-117° C.
Sources & evidence
- ORD record
- ord-1c8c7f892d674cfb870d8366e5993850
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07790312B2
Reaction notes
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