Reaction equation
[CH3:1][C:2]([CH3:21])([CH3:20])[C:3]#[C:4][C:5]#[C:6][Sn](CCCC)(CCCC)CCCC.[O-:22][S:23]([C:26]([F:29])([F:28])[F:27])(=[O:25])=[O:24].C([I+:32][C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)#N>>[O-:25][S:23]([C:26]([F:29])([F:28])[F:27])(=[O:24])=[O:22].[CH3:21][C:2]([CH3:1])([CH3:20])[C:3]#[C:4][C:5]#[C:6][I+:32][C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1Participants
3
Procedure
(5,5-dimethyl-1,3-hexadiynyl)tri-n-butylstannane was reacted with cyano(phenyliodonium) triflate as described in the preceding paragraph, with the product workup according to procedure 1) producing an 84% yield of 5,5-dimethyl-1,3-hexadiynyl(phenyliodonium) triflate.
Sources & evidence
- ORD record
- ord-c24db113699b430c98e40d268d29aee8
- Source dataset
- uspto-grants-1994_02
- Patent number
- US05286901
Linked notes
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