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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8750생성일: 2026년 10월 23일

Propanal → tert-Butyl 2-(1-hydroxyprop-1-yl)-1-oxo-8-azaspiro[4.5]decane-8-carboxylate

https://huagongshe.com/ko/reaction/8750

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참여 물질

역할이름HCID투입량
반응물PropanalHCID 527—
반응물Ammonium ChlorideHCID 25517—
반응물Tert-butyl 1-oxo-8-azaspiro(4.5)decane-8-carboxylateHCID 10848487—
반응물Lithium diisopropylamide mono(tetrahydrofuran)HCID 10997623—
용매Diethyl EtherHCID 3283—
생성물tert-Butyl 2-(1-hydroxyprop-1-yl)-1-oxo-8-azaspiro[4.5]decane-8-carboxylateHCID 21983945120.9%

반응 조건

온도-78 °C

반응 단계

tert-Butyl 1-oxo-8-azaspiro[4.5]decane-8-carboxylate from Step G (4.5 g, 17.8 mmol) was dried by evaporating with toluene (10 mL) three times in vacuo, dissolved in tetrahydrofuran (100 mL), and cooled to −78° C. To this solution was added lithium diisopropylamide mono(tetrahydrofuran) (24 mL, 36 mmol, 1.5 M in cyclohexane). The reaction mixture was stirred for 30 min at −78° C. before adding propionaldehyde (2.6 mL, 36 mmol). After 5 min, the reaction mixture was diluted with diethyl ether, poured into saturated ammonium chloride, and extracted three times with diethyl ether. The organic layers were combined, washed with brine, dried over sodium sulfate, filtered, and concentrated to afford 6.7 g of a clear oil. The residue was purified by flash chromatography eluting with 20–30% ethyl acetate in hexanes to give the title compound (4.75 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091211B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-f4d34c0f487347f9a801ff3387bd1e3d
출처 메모uspto-grants-2006_08