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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1177720생성일: 2026년 10월 27일

Di-tert-butyl dicarbonate → Methyl 2-(bis((tert-butoxy)carbonyl)amino)prop-2-enoate

https://huagongshe.com/reaction/1177720

반응식

참여 물질

역할이름HCID투입량
반응물Di-tert-butyl dicarbonateHCID 90495—
반응물Methyl N-(tert-butoxycarbonyl)serinateHCID 495564—
반응물2-(Di-tert-butoxycarbonylamino)-3-tert-butoxycarbonyloxy-propionic acid methyl esterHCID 58864266—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매AcetonitrileHCID 6342—
생성물Methyl 2-(bis((tert-butoxy)carbonyl)amino)prop-2-enoateHCID 10870342—

반응 단계

To a solution of 2-tert-butoxycarbonylamino-3-hydroxy-propionic acid methyl ester (10.0 g, 39 mmol) and di-tert-butyl-dicarbonate (21.8 g, 2.6 equiv.) in acetonitrile (40 mL) was added 4-dimethylaminopyridine (0.48 g, 0.1 equiv) at room temperature. The solution was stirred overnight and concentrated. The residue was dissolved in diethyl ether, washed sequentially with 1 M potassium hydrogen sulfate (2×), saturated sodium bicarbonate, brine, dried over magnesium sulfate, and concentrated to give 15.6 g (quant.) as an oil. Inspection of the 1H NMR showed a mixture of the title compound and 2-(di-tert-butoxycarbonylamino)-3-tert-butoxycarbonyloxy-propionic acid methyl ester. As it was later found that both react with secondary amines to give the same products, the mixture was used without separation. 2-(Di-tert-butoxycarbonylamino)-acrylic acid methyl ester: 1H-NMR (CDCl3) δ 1.45 (s, 18H), 3.78 (s, 3H), 5.63 (s, 1H), 6.33 (s, 1H). Mass spec.: 324.14 (M+Na)+. 2-(Di-tert-butoxycarbonylamino)-3-tert-butoxycarbonyloxy-propionic acid methyl ester: 1H-NMR (CDCl3, 500 MHz) δ 1.46 (s, 9H), 1.49 (s, 18H), 3.72 (s, 3H), 4.42 (dd, J=11.6, 9.2, 1H), 4.75 (dd, J=11.3, 4.6, 1H), 5.30 (dd, J=9.2, 4.6, 1H). Mass spec.: 442.21 (M+Na)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07842808B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-cfc12a12e08e43a1940843127c115370
출처 메모uspto-grants-2010_11