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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4593생성일: 2026년 10월 23일

Hydrochloric Acid → (2-Carbamoylethyl)-alpha-naphthoxymalonic acid diethyl ester

https://huagongshe.com/ko/reaction/4593

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물AcrylamideHCID 6579—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물4-Carbamoyl-2(R,S)-alpha-naphthoxybutyric acidHCID 23049649—
반응물alpha-Naphthoxymalonic acid diethyl esterHCID 54105534—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물(2-Carbamoylethyl)-alpha-naphthoxymalonic acid diethyl esterHCID 54384256—

반응 단계

4-Carbamoyl-2(R,S)-α-naphthoxybutyric acid: 1.49 ml of 1,8-diazabicyclo[5.4.0]undec-7-ene are added to a solution of 3 g of α-naphthoxymalonic acid diethyl ester (Example 36a) and 0.71 g of acrylamide in 5 ml of acetonitrile and the whole is stirred at room temperature for 24 hours. 25 ml of water are added to the reaction mixture, which is adjusted to pH 2 with 2N hydrochloric acid and extracted with ether. The ethereal phases are washed with water and brine, dried over sodium sulphate and concentrated by evaporation, leaving (2-carbamoylethyl)-α-naphthoxymalonic acid diethyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04727060
출처 데이터셋uspto-grants-1988_02
ORD IDord-822d95ff4f2445239bc38f50ab6bd0a8
출처 메모uspto-grants-1988_02