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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881386Generated: October 26, 2026

4-Benzoylbenzoic acid → Tri-n-butyl-(4-benzoyl-benzoyloxy)-tin

https://huagongshe.com/reaction/1881386

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzoylbenzoic acidHCID 69147—
ReactantTributyltin methoxideHCID 16683411—
Solvent1,2-DichloroethaneHCID 11—
ProductTri-n-butyl-(4-benzoyl-benzoyloxy)-tinHCID 6850874641.9%

Reaction Steps

In a 50 ml dry three-neck-flask, 2.0 g (8.8 mmol) 4-benzoylbenzoic acid in 30 ml 1,2-dichlorethane are suspended under argon flow and heated to reflux. 2.8 g (8.8 mmol) tri-n-butylmethoxy tin are added slowly in the course of 0.5 h. The conversion is complete according to the 1H-NMR-spectrum. The slightly turbid hot solution is filtered, cooled and concentrated. 3.6 g of the crude product are obtained as yellowish oil. 2.4 g thereof are heated in a bulb-to-bulb distillation apparatus (0.03 mbar) and distilled at 190° C. 1.9 g of the title product is obtained as colorless oil. The structure is confirmed by 1H-NMR and 13C-NMR-spectra.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318830B2
Source datasetuspto-grants-2012_11
ORD IDord-e127b5a293164734a91d62ff9df2e165
Source noteuspto-grants-2012_11