Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70724Generated: October 26, 2026

Water → Benzyl(dibutyl)chlorostannane

https://huagongshe.com/reaction/70724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantDibutyltin dichlorideHCID 12688—
ReactantAmmonium ChlorideHCID 25517—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl(dibutyl)chlorostannaneHCID 14517507—

Reaction Steps

In a round-bottom two-necked flask equipped with a condenser and a dropping funnel, 31.25 mmol (9.5 g) of dibutyltindichloride were dissolved in 25 ml of tetrahydrofurane (THF). Then 125.1 mmol (8.18 g) of zinc (zinc granules: −30+100 mesh, Sigma-Aldrich) and 50 ml of water saturated with NH4Cl were added. With vigorous stirring 125.1 mmol (21.4 g) of benzylbromide (in 1:1 stoichometric ratio with respect to zinc) were added drop wise at a rate sufficient to keep temperature below 27° C. The reaction flask was cooled down with ice. First a brown benzyldibutyltin chloride was formed as an intermediate. The addition took about 30 min. The resulting heterogeneous colorless mixture was stirred for a further 60-120 min to complete disappearance of Zn powder. The organic layer was separated, washed with saturated aqueous NaCl and dried over MgSO4. Solvent was removed by distillation under reduced pressure up to 45° C. for 5 hours. An oil like liquid remained, which was distilled under vacuum to afford the pure compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822622B2
Source datasetuspto-grants-2014_09
ORD IDord-df8e5aa4604e48dbb46fbd1895d4837c
Source noteuspto-grants-2014_09