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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177498Generated: November 1, 2026

Tributylstannane → Tributyl(1-(4-fluorophenyl)vinyl)stannane

https://huagongshe.com/reaction/1177498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylstannaneHCID 5948—
ReactantDiisopropylamineHCID 7912—
ReactantTriethylamineHCID 8471—
Reactant4'-FluoroacetophenoneHCID 9828—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductTributyl(1-(4-fluorophenyl)vinyl)stannaneHCID 67111781—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of diisopropylamine (1.39 mL, 10.1 mmol) in 20 mL THF at 0° C. was added butyllithium (4.02 mL, 10.0 mmol). After 10 min, tributylstannane (2.45 mL, 9.23 mmol) was added. After 10 min, the reaction mixture was cooled to −78° C. and a solution of 1-(4-fluorophenyl)ethanone (1.09 mL, 9.05 mmol) in 10 mL THF was added slowly by syringe in portions over 10 min. After 10 min, triethylamine (9.43 mL, 67.9 mmol) and methanesulfonyl chloride (2.80 mL, 36.2 mmol) was added and the bath allowed to expire overnight. The reaction mixture was treated with 50 mL hexanes and filtered, rinsing with hexanes. The filtrate was extracted with ACN, and the hexanes layer was dried over sodium sulfate, filtered, and concentrated. Purification with C-18 silica gel, eluting with DCM/ACN, gave tributyl(1-(4-fluorophenyl)vinyl)stannane as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842685B2
Source datasetuspto-grants-2010_11
ORD IDord-3066f3183c6646c8be70942bba9e771b
Source noteuspto-grants-2010_11