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HRID 374529作成日:2026年10月25日

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

https://huagongshe.com/reaction/374529

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物5(2H)-Oxazolone, 4-(4-chlorophenyl)-2-(trifluoromethyl)-HCID 11065291—
反応物HCID 54097949HCID 54097949—
溶媒Hydrochloric AcidHCID 313—
溶媒TolueneHCID 1140—
溶媒Diethyl EtherHCID 3283—
生成物2-[1-(5-Bromo-3-Thienyl)-2-Nitroethyl]-4-(p-Chlorophenyl)-2-(Trifluoromethyl)-3-Oxazolin-5-OneHCID 19419298—

反応手順

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 (10.0 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05480902
出典データセットuspto-grants-1996_01
ORD IDord-1d804fda3f4a48829d05b874f762e3a7
出典メモuspto-grants-1996_01