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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1939688Generated: October 25, 2026

Tributylstannane → 1-Fluoro-3-(4-chlorophenyl)-3-methyl-1-tributylstannyl-1-butene

https://huagongshe.com/reaction/1939688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylstannaneHCID 5948—
ReactantAzobisisobutyronitrileHCID 6547—
Reactant1-Fluoro-1-phenylsulfonyl-3-methyl-3-(4-chlorophenyl)-1-buteneHCID 53860513—
SolventCyclohexaneHCID 8078—
Product1-Fluoro-3-(4-chlorophenyl)-3-methyl-1-tributylstannyl-1-buteneHCID 67632345—

Reaction Steps

Under a nitrogen atmosphere, a stirring solution of 22.7 grams (0.067 mole) of 1-fluoro-1-phenylsulfonyl-3-methyl-3-(4-chlorophenyl)-1-butene, 42.0 grams (0.14 mole) of tributyltin hydride, and 0.5 gram (catalyst) of azobis-isobutyronitrile in 700 mL of cyclohexane is heated at reflux for about three hours. After this time the reaction mixture is cooled to ambient temperature, and 125 mL of silica gel is added. The mixture is concentrated under reduced pressure, and the residue is subjected to column chromatography. The product-containing fractions are combined and concentrated under reduced pressure, yielding 1-fluoro-3-(4-chlorophenyl)-3-methyl-1-tributylstannyl-1-butene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05696259
Source datasetuspto-grants-1997_12
ORD IDord-26be9e32081c4ba6a77a63b8dfa98cd8
Source noteuspto-grants-1997_12