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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2038376Generated: November 1, 2026

Bromine → Ethyl 5-bromo-4-(3-cyano-4-fluorophenyl)-1,3-thiazole-2-carboxylate

https://huagongshe.com/reaction/2038376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium ThiosulfateHCID 24477—
ReactantPotassium AcetateHCID 517044—
ReactantEthyl 4-(3-cyano-4-fluorophenyl)-1,3-thiazole-2-carboxylateHCID 70801688—
SolventAcetic AcidHCID 176—
ProductEthyl 5-bromo-4-(3-cyano-4-fluorophenyl)-1,3-thiazole-2-carboxylateHCID 70801513—

Reaction Conditions

Temperature100 °C

Reaction Steps

At room temperature, 8.10 g (50.6 mmol) of bromine and 4.97 g (50.6 mmol) of potassium acetate are added to 1.40 g (5.07 mmol) of the compound from Example 28A in 80 ml of conc. acetic acid. The mixture is stirred at 100° C. for 48 h, whereby after 24 and 36 h, bromine (in each case 4.05 g, 25.3 mmol) and potassium acetate (in each case 2.49 g, 25.3 mmol) are again added. A 1M aqueous sodium thiosulfate solution is subsequently added, and the reaction solution is extracted with dichloromethane. The combined organic phases are dried over MgSO4, filtered and concentrated under reduced pressure. The crude product is purified by flash chromatography (mobile phase: cyclohexane/ethyl acetate 20:1→10:1). 1.55 g (84% of theory) of the title compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575357B2
Source datasetuspto-grants-2013_11
ORD IDord-852ec8dcc0cf43d3b493911a5e4724a9
Source noteuspto-grants-2013_11