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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262816Generated: November 1, 2026

Benzoyl chloride → HCID 13318174, compound

https://huagongshe.com/reaction/1262816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantHCID 54703303HCID 54703303—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 13318174HCID 1331817495%

Reaction Conditions

Temperature10 °C

Reaction Steps

A mixture of di-isopropyl 3-methyl-4-hydroxy-2,5-thiophene-dicarboxylate (656 g, 2.30 mol), triethylamine (297 g, 2.98 mol) and dioxane (2 l) was cooled with ice to about 10° C. The solution was added, while stirring, with benzoyl chloride (351 g, 2.5 mol) over about 10 minutes, followed by further stirring for 30 minutes at room temperature. After removing the precipitate of triethylamine hydrochloride salt by filtration, the solution was distilled in vacuo to remove dioxane. Toluene was then added to the remaining residue, and the solution was washed with 5% aqueous sodium bicarbonate and water, and then dried over MgSO4. The solvent was removed by distillation to give almost pure di-isopropyl 3-methyl-4-benzoyloxy-2,5-thiophene dicarboxylate (851 g, 95%). nD10 1.5499.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04454131
Source datasetuspto-grants-1984_06
ORD IDord-ce623c9f9d4e478eb4717369f83e9235
Source noteuspto-grants-1984_06