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HRID 249992作成日:2026年10月26日

Formamide → 4-Methyl-1,3-oxazole-5-carboxylic acid

https://huagongshe.com/reaction/249992

反応式

関与物質

役割名称HCID仕込み量
反応物FormamideHCID 713—
反応物Ethyl 2-chloroacetoacetateHCID 11858—
反応物Sodium HydroxideHCID 14798—
溶媒Ethyl AcetateHCID 8857—
生成物4-Methyl-1,3-oxazole-5-carboxylic acidHCID 29231164.5%

反応条件

温度120 °C

反応手順

Ethyl-2-chloroacetoacetate (1 wt; 1 eq., 1000 g) was aged with formamide (0.68 vol; ca. 2.8 eq.) and the resulting solution was heated to 120° C. After 5 hours the mixture was allowed to cool to room temperature and allowed to age under nitrogen over night. The mixture was treated with NaOH (3 M, 6 vol, reaction moderately exothermic) and stirred at room temperature for 4 hours. Ethyl acetate (6 vol) was added and the phases allowed to separate. The organic layer was discarded while the aqueous was acidified with conc. (32%) aqueous HCl to pH 2 (ca. 2.0 vol). A precipitate started to form. The suspension was treated with AcOEt (8 vol) and vigorously stirred until the bulk of the precipitate had dissolved. The aqueous phase was further extracted with AcOEt twice (6 vol each) and the combined organic layers distilled to low volume (again a suspension was observed at low volume). Fresh AcOEt (8 vol) was added and the mixture evaporated to dryness. The collected solid was placed in the oven at 40° C. over night under reduced pressure to give 4-methyl-1,3-oxazole-5-carboxylic acid (498 g, 64.5%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07863299B2
出典データセットuspto-grants-2011_01
ORD IDord-01dad1690b0744549eaec54f39211a0f
出典メモuspto-grants-2011_01