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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 128504생성일: 2026년 10월 24일

Toluene → Allyl 6beta-[(allyloxycarbonyl)acetamido]-2,2-dimethylpenam-3-carboxylate

https://huagongshe.com/ko/reaction/128504

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물6-Aminopenicillanic acidHCID 11082—
반응물Malonic acid monoallyl esterHCID 10888030—
용매ChloroformHCID 6212—
생성물Allyl 6beta-[(allyloxycarbonyl)acetamido]-2,2-dimethylpenam-3-carboxylateHCID 6778540346%

반응 단계

In a manner similar to that described for Example 1, method A, the title compound (3.53 g, 46%) was prepared from malonic acid monoallyl ester (2.88 g, 20 mmol) and 6-aminopenicillanic acid (4.33 g, 20 mmol) as colorless crystals: m.p. 59°-60° C. (toluene); IR (CHCl3) 1790, 1730, 1685 cm-1; 1 H NMR (CDCl3) δ 1.51 and 1.67 (each 3H, s, C2 -(CH3)2), 3.35-3.47 (2H, m, COCH2CO), 4.48 (1H, s, C3 -H), 4.60-4.70 (4H, m, 2xOCH2CH=CH2), 5.22-5.42 (4H, m, 2xOCH2CH=CH2), 5.56 (1H, d, J=4Hz, C5-H), 5.75 (1H, dd, J=4 and 9Hz, C6 -H), 5.84-6.00 (2H, m, 2xOCH2CH=CH2), 8.03 (1H, d, J=9Hz, NH).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05464616
출처 데이터셋uspto-grants-1995_11
ORD IDord-67b89f0dcdb347d2ad2f4ceb4b51d66d
출처 메모uspto-grants-1995_11