Methanesulfonyl chloride → Methanesulfonic acid 4-(4-trifluoromethyl-phenyl)-but-3-ynyl ester
Reaction equation
[F:1][C:2]([F:15])([F:14])[C:3]1[CH:8]=[CH:7][C:6]([C:9]#[C:10][CH2:11][CH2:12][OH:13])=[CH:5][CH:4]=1.[CH3:16][S:17](Cl)(=[O:19])=[O:18]>>[F:1][C:2]([F:14])([F:15])[C:3]1[CH:4]=[CH:5][C:6]([C:9]#[C:10][CH2:11][CH2:12][O:13][S:17]([CH3:16])(=[O:19])=[O:18])=[CH:7][CH:8]=1Participants
3
Procedure
In analogy to the procedure described in example 1G], 4-(4-trifluoromethyl-phenyl)-but-3-yn-1-ol and methanesulfonyl chloride gave the title compound as light yellow oil.
Sources & evidence
- ORD record
- ord-b81397ea6910461fa3575933154c1ed9
- Source dataset
- uspto-grants-2007_08
- Patent number
- US07253192B2
Reaction notes
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