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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 241787생성일: 2026년 10월 26일

3-Methylenecyclobutanecarboxylic acid → tert-butyl N-(3-methylidenecyclobutyl)carbamate

https://huagongshe.com/reaction/241787

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참여 물질

역할이름HCID투입량
반응물3-Methylenecyclobutanecarboxylic acidHCID 27475—
반응물Sodium AzideHCID 33557—
반응물Di-tert-butyl dicarbonateHCID 90495—
촉매Tetrabutylammonium BromideHCID 74236—
촉매Zinc trifluoromethanesulfonateHCID 104671—
용매TetrahydrofuranHCID 8028—
생성물tert-butyl N-(3-methylidenecyclobutyl)carbamateHCID 2887536934.9%

반응 조건

온도40 °C

반응 단계

To a stirring solution of 3-methylene-cyclobutane carboxylic acid (1.0 g, 8.9 mmol) in THF (90 mL) was added NaN3 (2.0 g, 31.1 mmol), followed by tetrabutyl ammonium bromide (0.48 g, 1.5 mmol) and Zn(OTf)2 (0.1 g, 0.3 mmol), and the reaction mixture was heated to 40° C. Boc2O (2.1 g, 9.8 mmol) was then added at once, and the reaction was heated at 45° C. overnight. The reaction was then cooled to 0° C. and was quenched with 10% aq. NaNO2 (180 mL). The THF was evaporated and the aqueous layer was extracted with EtOAc (180 mL). The organic layer was washed with 5% aq. NaHCO3 (2×20 mL), brine (30 ml), dried over Na2SO4, filtered and concentrated to dryness to yield a crude, which was purified by flash chromatography (silica gel/hexanes:ethyl acetate: 0-90%) to yield the desired N-Boc-3-methylene-cyclobutanamine (0.57 g, 3.1 mmol, 34.9% yield): 1H NMR (250 MHz, CDCl3) δ 4.83 (s, 2H), 4.79 (bs, 1H), 4.05-4.23 (m, 1H), 2.92-3.11 (m, 2H), 2.50-2.65 (m, 2H), 1.44 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653042B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-82b8ff5d172746dc9d5ba65e8069df24
출처 메모uspto-grants-2014_02