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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Cyclohexanecarboxaldehyde, 4-(1,1-dimethylethyl)- | HCID 88655 | — |
| 반응물 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 반응물 | 1-(Methoxycarbonylmethyl)-spiro[indoline-3,4'-piperidin]-2-one | HCID 59164537 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 생성물 | 1-(Methylcarbonyloxy-methyl)-5-(4-t-butyl-cyclohexyl-methyl)-spiro[indoline-3,4'-piperidin]-2-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07655670B2 |
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| 출처 데이터셋 | uspto-grants-2010_02 |
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| ORD ID | ord-9bdd9ad7531a482f8c6d307dfa0e4014 |
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| 출처 메모 | uspto-grants-2010_02 |
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