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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54259Generated: October 28, 2026

Water → 3-(4-Fluorophenyl)-3-methyl-1-tributylstannyl-1-butene

https://huagongshe.com/reaction/54259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant3-(4-Fluorophenyl)-3-methyl-1-iodo-1-tributylstannylbutaneHCID 21467967—
SolventTetrahydrofuranHCID 8028—
Product3-(4-Fluorophenyl)-3-methyl-1-tributylstannyl-1-buteneHCID 6763152488.2%

Reaction Steps

Under a nitrogen atmosphere, a stirred solution of 17.2 grams (0.030 mole ) of 3-(4-fluorophenyl)-3-methyl-1-iodo-1-tributylstannylbutane and 13.7 grams (0.090 mole) of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in 100 mL of tetrahydrofuran is heated at reflux for about 18 hours. The reaction mixture is cooled and poured into about 500 mL of water. The mixture is then made acidic with aqueous 2N hydrochloric acid and extracted with three 200 mL portions of diethyl ether. The combined extracts are dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure to a residue. The residue is subjected to column chromatography on silica gel, using 5% methylene chloride in petroleum ether as the eluant. The product-containing fractions are combined and concentrated under reduced pressure, yielding 12.0 grams of 3-(4-fluorophenyl)-3-methyl-1-tributylstannyl-1-butene. The NMR spectrum is consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05622954
Source datasetuspto-grants-1997_04
ORD IDord-8160a919727843de88cd84d6a77a8bce
Source noteuspto-grants-1997_04