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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 417728생성일: 2026년 10월 26일

(Dimethyl sulfide)trihydroboron → Ethyl 5-oxa-6-azaspiro[3.4]octane-7-carboxylate

https://huagongshe.com/reaction/417728

반응식

참여 물질

역할이름HCID투입량
반응물(Dimethyl sulfide)trihydroboronHCID 12423031—
반응물Ethyl 5-oxa-6-azaspiro[3.4]oct-6-ene-7-carboxylateHCID 59611573—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 5-oxa-6-azaspiro[3.4]octane-7-carboxylateHCID 5961153829%

반응 단계

To a solution of crude 5-oxa-6-aza-spiro[3.4]oct-6-ene-7-carboxylic acid ethyl ester (7.5 g, <40.9 mmol) in tetrahydrofuran (270 mL) at 0° C. was slowly added a solution of borane-dimethyl sulfide complex (10 M in THF, 16.4 mL, 164 mmol). The reaction was allowed to warm to room temperature overnight then recooled to 0° C., and quenched by the careful addition of water. The mixture was diluted with ethyl acetate, washed with water and brine, dried (MgSO4), and concentrated to yield a large amount of white solids. These solids were thoroughly triturated three times with dichloromethane (150 mL). The combined dichloromethane washings were concentrated and the resulting oil was purified by flash chromatography to yield 5-oxa-6-aza-spiro[3.4]octane-7-carboxylic acid ethyl ester (1.08 g, 29% over 2 steps). 1H-NMR: 400 MHz, (CDCl3) δ: 8.01-7.95 (br, 1H), 4.39-4.28 (m, 2H), 4.18-4.10 (m, 1H), 2.80-2.75 (m, 1H), 2.62-2.49 (m, 2H), 2.37-2.29 (m, 1H), 2.25-2.17 (m, 1H), 2.13-1.95 (m, 1H), 1.88-1.79 (m, 1H), 1.68-1.56 (m, 1H), 1.34 (t, J=7.1 Hz, 3H) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08088368B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-1148a1d2cd2548f7a297f340e9ce9874
출처 메모uspto-grants-2012_01