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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410009Generated: October 31, 2026

Tributyltin Chloride → HCID 67060786, compound

https://huagongshe.com/reaction/410009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
Reactant2,2'-BifuranHCID 80006—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67060786HCID 6706078660%

Reaction Steps

A solution of n-BuLi (7.7 mL, of 2.5M in hexanes, 19.2 mmol, 1.3 equivalents) was added dropwise to a solution of bifuran (2 g, 14.9 mmol) in dry THF (100 mL) at −78° C. under N2. The mixture was allowed to come to room temperature and stirred for 1 h. To the white suspension was added dropwise Bu3SnCl (4 mL, 14.9 mmol) at 0° C. and the reaction was allowed to reach room temperature and stirred for 2 h. The mixture was extracted with hexane, dried (MgSO4) and evaporated. Seperation by chromatography using bacified silica (Et3N) and hexane gave 1 (3.8 g, 60% yield) as a colorless oil. 1H NMR (300 MHz, CDCl3): δ 0.85-0.91 (t, J=7.3 Hz, 9H), 1.03-1.13 (m, 6H), 1.26-1.39 (m, 6H), 1.48-1.63 (m, 6H), 6.40-6.42 (m, 1H), 6.50 (d, J=3.3 Hz, 1H), 6.57 (dd, J=3.3, 6.0 Hz, 2H), 7.34 (dd, J=0.7, 1.8 Hz, 1H) ppm. 13C NMR (300 MHz, CDCl3): δ 10.2, 13.7, 27.2, 28.9, 104.6, 105.0, 111.3, 123.0, 141.4, 147.5, 151.0, 160.9 ppm

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759550B2
Source datasetuspto-grants-2014_06
ORD IDord-a051b7894e01484194bf93ef5ed7f214
Source noteuspto-grants-2014_06