돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1252364생성일: 2026년 10월 26일

Butyl 2-acetamido-3-phenylprop-2-enoate → Methyl alpha-acetamidocinnamate

https://huagongshe.com/reaction/1252364

반응식

참여 물질

역할이름HCID투입량
반응물Butyl 2-acetamido-3-phenylprop-2-enoateHCID 54426445—
용매O-XyleneHCID 7237—
생성물Methyl alpha-acetamidocinnamateHCID 340163—

반응 단계

Following the procedure of step (iv) of Example 1 but using a 300-ml portion of the o-xylene solution of butyl α-acetamidocinnamate as obtained in step (iii) of Example 8 in place of the o-xylene solution of methyl α-acetamidocinnamate, the hydrogenation reaction was carried out in the same manner as in said step (iv) of Example 1. The conversion of butyl α-acetamidocinnamate was 100 percent and the selectivity toward N-acetyl-DL-phenylalanine butyl ester 99 mole percent. The palladium-on-carbon catalyst was filtered off from the reaction mixture, the filtrate was concentrated under reduced pressure and the residue was purified by column chromatography to give 32 g of N-acetyl-DL-phenylalanine butyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04743547
출처 데이터셋uspto-grants-1988_05
ORD IDord-2edb202367394680b9ad0a47b0a936c1
출처 메모uspto-grants-1988_05