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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132017생성일: 2026년 10월 24일

Acetic Acid → Entacapone Impurity 55

https://huagongshe.com/ko/reaction/132017

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물PiperidineHCID 8082—
반응물3-Ethoxy-4-hydroxy-5-nitrobenzaldehydeHCID 584878—
반응물2-cyano-N,N-bis(ethylamino)acetamideHCID 86611404—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물Entacapone Impurity 55HCID 69218750172.7%

반응 단계

A flask was charged with 3-ethoxy-4-hydroxy-5-nitrobenzaldehyde (20 g, 0.0947 mole) (formula 2 where R is ethyl) and N,N-diethylaminocyanoacetamide (formula (3)) (14.6 g, 0.1042 mol), acetic acid (3.13 g), and piperidine (4.45 g), along with toluene (200 mL), and was heated to a reflux temperature of about 100-115° C. with continuous removal of water azeotrophically for about 15 hours. After the reaction was complete, the reaction mixture was concentrated to a volume of 20-30 mL, quenched into dilute hydrochloric acid and chilled water (200 mL), and stirred for 60 minutes. The precipitated solid was filtered and dried to provide 30 g (95% yield, HPLC purity of 94% (including isomer)) of N,N-diethyl-2-cyano-3-(-3-ethoxy-4-hydroxy-5-nitrophenyl)acrylamide. The product was used as such directly to the next stage. MR=110.0-117.2° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07385072B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-835738e53b76464a917b4f815a4aaf91
출처 메모uspto-grants-2008_06