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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396547Generated: October 26, 2026

Triethylamine → 2-[1-(5-Bromo-3-Thienyl)-2-Nitroethyl]-4-(p-Chlorophenyl)-2-(Trifluoromethyl)-3-Oxazolin-5-One

https://huagongshe.com/reaction/2396547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5(2H)-Oxazolone, 4-(4-chlorophenyl)-2-(trifluoromethyl)-HCID 11065291—
Reactant2-Bromo-4-(2-nitrovinyl)thiopheneHCID 54097949—
SolventHydrochloric AcidHCID 313—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Product2-[1-(5-Bromo-3-Thienyl)-2-Nitroethyl]-4-(p-Chlorophenyl)-2-(Trifluoromethyl)-3-Oxazolin-5-OneHCID 19419298—

Reaction Steps

A solution of triethylamine (0.30 g, 3 mmol) in toluene is added to a solution of 4-(p-chlorophenyl)-2-(trifluoromethyl)-3-oxazolin-5-one (10.00 g, 38 mmol) and 2-bromo-4-(2-nitrovinyl)thiophene (8.98 g, 32 mmol) in toluene at 0° C. The reaction mixture is warmed to room temperature and diluted with dilute hydrochloric acid and ether. The organic layer is separated, dried over MgSO4, concentrated in vacuo, diluted with hexane, stirred at reflux, cooled to room temperature and decanted to obtain a clear solution. The solution is concentrated in vacuo and chromatographed to give the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05492925
Source datasetuspto-grants-1996_02
ORD IDord-afbb082226d241a0b9f6ebad82186e03
Source noteuspto-grants-1996_02