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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1441677생성일: 2026년 10월 26일

Acetic Acid → 1-(Methylcarbonyloxy-methyl)-5-(4-t-butyl-cyclohexyl-methyl)-spiro[indoline-3,4'-piperidin]-2-one

https://huagongshe.com/reaction/1441677

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Cyclohexanecarboxaldehyde, 4-(1,1-dimethylethyl)-HCID 88655—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물1-(Methoxycarbonylmethyl)-spiro[indoline-3,4'-piperidin]-2-oneHCID 59164537—
용매1,2-DichloroethaneHCID 11—
생성물1-(Methylcarbonyloxy-methyl)-5-(4-t-butyl-cyclohexyl-methyl)-spiro[indoline-3,4'-piperidin]-2-oneHCID 68542360—

반응 단계

1-(Methoxycarbonyl-methyl)-spiro[indoline-3,4′-piperidin]-2-one (0.0137 g, 0.049 mmol) and 4-tert-butyl-cyclohexanecarbaldehyde (0.01 g, 0.06 mmol) were dissolved in dry 1,2-dichloroethane (1.5 mL). To the reaction mixture was then added glacial acetic acid (0.003 g, 0.049 mmol) under nitrogen atmosphere and the reaction mixture was stirred at room temperature for 30 minutes. To the reaction mixture was then added, at room temperature, sodium triacetoxyborohydride (0.018 g, 0.084 mmol) under nitrogen atmosphere and the reaction mixture was stirred at room temperature for 18 hours. The reaction mixture was then partitioned with aqueous NaHCO3 and dichloromethane. The organic layer was washed with brine, dried with Na2SO4, filtered and the solvent evaporated in vacuo to yield a crude oil. The crude oil was purified via flash chromatography (4.5% ammonia 2.0 M in methanol/dichloromethane) to yield the title compound as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07655670B2
출처 데이터셋uspto-grants-2010_02
ORD IDord-9bdd9ad7531a482f8c6d307dfa0e4014
출처 메모uspto-grants-2010_02