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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53977Generated: October 27, 2026

Sodium hydride → Ethyl 3-(5-bromobenzo[b]thien-2-yl)-2-ethoxycarbonyl-2-(4-methoxyphenyl)propionate

https://huagongshe.com/reaction/53977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantDiethyl 2-(4-methoxyphenyl)malonateHCID 2785178—
Reactant5-Bromo-2-(bromomethyl)benzo[b]thiopheneHCID 14819352—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(5-bromobenzo[b]thien-2-yl)-2-ethoxycarbonyl-2-(4-methoxyphenyl)propionateHCID 2184420292.4%

Reaction Steps

14.2 g of ethyl 2-ethoxycarbonyl-2-(4-methoxyphenyl)acetate was dissolved in 150 ml of tetrahydrofuran. 2.6 g of sodium hydride (oil type, 60%) was added to the above solution while stirring under ice cooling, and the stirring was continued for 20 minutes. To this was further added 17.2 g of 5-bromo-2-bromomethylbenzo[b]thiophene. After stirring at room temperature for 18 hours, the resulting reaction solution was mixed with ammonium chloride aqueous solution, and then extracted with ethyl acetate. After drying to distill off the solvent, the resulting residue was subjected to silica gel column chromatography using chloroform as an elution solvent, thereby obtaining 24.2 g of ethyl 3-(5-bromobenzo[b]thien-2-yl)-2-ethoxycarbonyl-2-(4-methoxyphenyl)propionate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05620991
Source datasetuspto-grants-1997_04
ORD IDord-dbde7cd1490149faa0abad586b4db122
Source noteuspto-grants-1997_04