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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254475Generated: November 1, 2026

Stannane, tributyl-3-thienyl- → HCID 19744835, compound

https://huagongshe.com/reaction/2254475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannane, tributyl-3-thienyl-HCID 10959689—
ReactantHCID 19744768HCID 19744768—
CatalystHCID 178418397HCID 178418397—
ProductHCID 19744835HCID 1974483577%

Reaction Steps

1.4 g of 3-bromomethylbenzaldehyde was dissolved in 3 ml of dimethylformamide, and the solution was added to 5 ml of a tetrahydrofuran solution of phenolate, prepared from 1.5 g of 3-bromophenol and 0.36 g of 60% oily sodium hydride. The mixture was stirred for 2 hours at room temperature. The solvent was evaporated, and water and ethyl acetate were added to the residue to extract it. The extract was worked up in a customary manner to give crude 3-(3-bromophenoxymethyl)benzaldehyde. When the same reaction as in Referential Example 12 was performed using 440 mg of the resulting aldehyde compound, 747 mg of tributyl(3-thienyl)stannane and 10 mg of tetrakis(triphenylphosphine)palladium, 341 mg (yield 77%) of 3-[3-(3-thienyl)phenoxymethyl)benzaldehyde was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05234946
Source datasetuspto-grants-1993_08
ORD IDord-c20ae219328f451abf0958ae9422edb1
Source noteuspto-grants-1993_08