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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 563940생성일: 2026년 10월 26일

Hydrochloric Acid → 4-Methyl-1,3-oxazole-5-carboxylic acid

https://huagongshe.com/reaction/563940

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium CarbonateHCID 10340—
반응물Ethyl 2-chloroacetoacetateHCID 11858—
반응물Ethyl 4-methyloxazole-5-carboxylateHCID 88558—
반응물Ammonium formateHCID 2723923—
용매Formic AcidHCID 284—
용매WaterHCID 962—
용매Sodium HydroxideHCID 14798—
생성물4-Methyl-1,3-oxazole-5-carboxylic acidHCID 292311—

반응 단계

A solution of 40.0 grams (0.243 mol, 1.0 eq) of 2-Chloro-3-oxo-butyric acid ethyl ester in 240 mL formic acid (99%) was stirred at room temperature in a 500 mL round bottom flask equipped with a H2O condenser. To this solution was added 80.0 grams (1.27 mmol, 5.2 eq) of ammonium formate. The solution was then heated to reflux for five hours. After cooling to room temperature, the solution was diluted with water (1 L) and neutralized with Na2CO3. The aqueous solution was then extracted three times with Et2O and the combined organic fractions were dried over MgSO4. After concentration, vacuum distillation (˜10 mmHg, b.p. 53° C.-61° C.) gave a mixture of starting material and 4-Methyl-oxazole-5-carboxylic acid ethyl ester as a colorless oil (21.7 grams). This mixture was dissolved in 100 mL of aqueous sodium hydroxide (2 N) and refluxed for 1 minute. The reaction was then poured onto ice and acidified with concentrated HCl and the known (Sen & Sengupta (1985) Ind. J. Chem. Section B: Org. Chem. Including Med. Chem. 24B(5):535-8) free acid precipitated as a white solid (6.04 grams, 20% overall yield) Mp: 241.4-242.6° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08067583B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-e06c82575c51497491332e727a5182bc
출처 메모uspto-grants-2011_11