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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566392Generated: November 1, 2026

Tributyltin Chloride → 5-(4-Methyl-2,6,7-trioxabicyclo[2,2,2]oct-1-yl)-2-[tri(n-butyl)stannyl]furan

https://huagongshe.com/reaction/566392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
Reactant2-(4-Methyl-2,6,7-trioxabicyclo[2,2,2]oct-1-yl)furanHCID 22609742—
SolventTetrahydrofuranHCID 8028—
Product5-(4-Methyl-2,6,7-trioxabicyclo[2,2,2]oct-1-yl)-2-[tri(n-butyl)stannyl]furanHCID 2260970895.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

2-(4-Methyl-2,6,7-trioxabicyclo[2,2,2]oct-1-yl)furan (2.0 g, 10.2 mmol) was dissolved in THF (20 ml) and the solution was cooled to −78° C. n-Buli (1.6M solution in hexanes, 7.7 ml, 12.32 mmol) was added and the mixture stirred at −78° C. for 30 min, allowed to warm to 0° C. for 20 min. and then recooled to −78° C. The tributyltin chloride (3.5 ml, 4.68 g, 14.4 mmol) was added and stirring was continued at −78° C. for 15 min. The mixture was allowed to warm gradually to room temperature and stirring continued for three days. The reaction was quenched by the addition of water, and extracted with ethyl acetate. This solution was washed with water, dried (MgSO4), and concentrated in vacuo to give the title compound as a yellow oil (4.7 g, 9.7 mmol, 95%); δH [2H6]DMSO 6.52 (1H,d), 6.38 (1H,d), 3.96 (6H,s), 0.77-1.63 (30H,m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06174889B1
Source datasetuspto-grants-2001_01
ORD IDord-fa73696acc7e4bb580ecbae151507658
Source noteuspto-grants-2001_01