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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643776Generated: October 31, 2026

Sodium Acetate → Ethyl 7-(Acetyloxy)-2-methyl-1-benzothiophene-5-carboxylate

https://huagongshe.com/reaction/1643776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
Reactant3-(Ethoxycarbonyl)-4-(5-methyl-3-thienyl)but-3-enoic AcidHCID 66755556—
SolventDichloromethaneHCID 6344—
SolventAcetic AnhydrideHCID 7918—
ProductEthyl 7-(Acetyloxy)-2-methyl-1-benzothiophene-5-carboxylateHCID 5956016642%

Reaction Steps

Sodium acetate (30 g, 0.36 mol) was added under vigorous stirring to a solution of 3-(ethoxycarbonyl)-4-(5-methyl-3-thienyl)but-3-enoic acid (30 g, 0.12 mol) in 300 mL of acetic anhydride. The reaction mixture was refluxed for 3 h and evaporated in vacuum (˜20 mmHg) at 70° C. until the solvent distillation ceased. The obtained crude product was suspended in 500 mL of dichloromethane. The suspension was filtered. The precipitate was washed by 250 mL of dichloromethane. The combined solutions were washed by 350 mL of a saturated aqueous solution of NaHCO3 and evaporated in vacuum to dryness. The obtained crude product was chromatographed on a layer of silica gel (250×150 mm) with hexane/ethyl acetate mixture (3:1) to give the desired product 14 g (50 mmol, 42%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119624B2
Source datasetuspto-grants-2012_02
ORD IDord-31a83d9989f5474481522699a3ab1489
Source noteuspto-grants-2012_02