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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 602327생성일: 2026년 10월 26일

Formaldehyde → 3-(5-Chlorothiophene-2-carbonyl)oxazolidine-5-carboxylic acid

https://huagongshe.com/reaction/602327

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물IsoserineHCID 11267—
반응물Sodium BicarbonateHCID 516892—
반응물5-Chlorothiophene-2-carbonyl ChlorideHCID 589223—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매Sodium HydroxideHCID 14798—
생성물3-(5-Chlorothiophene-2-carbonyl)oxazolidine-5-carboxylic acidHCID 58691249—

반응 단계

4.1 1.48 ml (19.9 mmol) of 37% aqueous formaldehyde solution are added to a solution of 2.00 g (19.0 mmol) of DL-isoserine in 10 ml of 1N aqueous sodium hydroxide solution. The resultant solution is left at 5° C. for 18 hours. A solution of 3.46 g (19.1 mmol) of 5-chlorothiophenecarbonyl chloride in 10 ml of acetone is added dropwise to this solution at an internal temperature of 0-5° C. During the dropwise addition, the pH is held at a value above 7 by addition of solid sodium hydrogencarbonate. When the addition is complete, the mixture is allowed to warm to room temperature, water is added, and the mixture is extracted with tert-butyl methyl ether The aqueous phase is acidified using 1N HCl and extracted with tert-butyl methyl ether. This organic phase is dried over sodium sulfate and evaporated, giving 3-(5-chlorothiophene-2-carbonyl)oxazolidine-5-carboxylic acid as a colourless solid; ESI 262.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07906516B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-f16f5ab193984ffc9ac0fa8a035495f7
출처 메모uspto-grants-2011_03