Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Butyl 2-acetamido-3-phenylprop-2-enoate → Methyl alpha-acetamidocinnamate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Butyl 2-acetamido-3-phenylprop-2-enoate | HCID 54426445 | — |
| 용매 | O-Xylene | HCID 7237 | — |
| 생성물 | Methyl alpha-acetamidocinnamate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04743547 |
| 출처 데이터셋 | uspto-grants-1988_05 |
| ORD ID | ord-2edb202367394680b9ad0a47b0a936c1 |
| 출처 메모 | uspto-grants-1988_05 |