3-Chloro-1-propyne → 2,3,5,6-Tetrafluoro-4-(2-propyn-1-yl)benzyl Alcohol
Reaction equation
Br[C:2]1[C:15]([F:16])=[C:14]([F:17])[C:5]([CH2:6][O:7]C2CCCCO2)=[C:4]([F:18])[C:3]=1[F:19].[CH2:20](Cl)[C:21]#[CH:22]>>[CH2:22]([C:2]1[C:3]([F:19])=[C:4]([F:18])[C:5]([CH2:6][OH:7])=[C:14]([F:17])[C:15]=1[F:16])[C:21]#[CH:20]Participants
3
Procedure
4-(Prop-2-yn-1-yl)-2,3,5,6-tetrafluorobenzyl alcohol was prepared from 2-[4-bromo-2,3,5,6-tetrafluorobenzyloxy)-tetrahydropyran and propargyl chloride, by a two stage procedure similar to that described in Example 4.
Sources & evidence
- ORD record
- ord-5ce9533c29f84242b8341dbcdb65a59f
- Source dataset
- uspto-grants-1992_07
- Patent number
- US05132469
Reaction notes
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