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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372808Generated: October 26, 2026

Tin tetrachloride → (2-Butyl-3-benzo[b]furanyl) (5-methoxy-2-thienyl)methanone

https://huagongshe.com/reaction/2372808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTin tetrachlorideHCID 24287—
Reactant2-ButylbenzofuranHCID 77951—
Reactant5-Methoxy-2-thiophenecarbonyl chlorideHCID 14721834—
SolventChloroformHCID 6212—
Product(2-Butyl-3-benzo[b]furanyl) (5-methoxy-2-thienyl)methanoneHCID 14721835—

Reaction Conditions

Temperature0 °C

Reaction Steps

3.0 g (17.2 mmol) 2-butylbenzo[b]furan were dissolved in 30 ml abs. chloroform, the solution was cooled to 0° C., and reacted with 3.6 g (20.4 mmol) 5-methoxy-2-thiophenecarbonyl chloride, dissolved in 5 ml abs. chloroform, and then, at a temperature between 0° and 3° C., 2.8 ml SnCl4 were added dropwise. Stirring for 2 hours at 0° C. followed. The reaction mixture was evacuated under ice-cooling over 50 ml 2N HCl, the phases were separated and the aqueous phase thoroughly extracted with ether. The chloroform and ether phases were each washed with 50 ml 2N NaOH, combined, dried over sodium sulphate and evaporated. The crude product was quickly distilled.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05100911
Source datasetuspto-grants-1992_03
ORD IDord-3a67cd2fe798453f90f8e3841c0c8efd
Source noteuspto-grants-1992_03