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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771926Generated: November 3, 2026

Ethanol → Ethyl 5-bromothiophene-3-carboxylate

https://huagongshe.com/reaction/1771926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant5-Bromothiophene-3-carboxylic acidHCID 12039978—
SolventSulfuric AcidHCID 1118—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
ProductEthyl 5-bromothiophene-3-carboxylateHCID 15293216—

Reaction Steps

5-bromo-thiophene-3-carboxylic acid (18.2 g, 0.09 mol) was dissolved in absolute ethanol (150 ml) and H2SO4 (5 ml), and the mixture was refluxed for 5 hours. The mixture was concentrated under vacuum to give a yellow oil, then diluted with a mixture of ethyl acetate (100 ml) and saturated brine (200 ml), and mixed, let standing for layer separation. The aqueous layer was washed with ethyl acetate (25 ml twice). The extract and the organic layer was adjusted with Na2CO3 (10%) to pH=8, and the organic phase was separated and washed with saturated brine to pH=7, dried over anhydrous Na2SO4 over night. The organic layer was concentrated under reduced pressure to give 5-bromo-thiophene-3-carboxylic acid ethyl ester as yellow oil (15 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249154B2
Source datasetuspto-grants-2016_02
ORD IDord-a1f7535c79e04bbcb9dbc0efbf0e3c0d
Source noteuspto-grants-2016_02