Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1,6-Dioxaspiro[2.5]octane → Benzyl({1-[(4-hydroxytetrahydro-2H-pyran-4-yl)methyl]piperidin-4-yl}methyl)carbamate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1,6-Dioxaspiro[2.5]octane | HCID 160439 | — |
| 반응물 | Benzyl (piperidin-4-ylmethyl)carbamate | HCID 14809798 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | Benzyl({1-[(4-hydroxytetrahydro-2H-pyran-4-yl)methyl]piperidin-4-yl}methyl)carbamate | HCID 59255048 | 49.4% |
반응 단계
A mixture of benzyl(piperidin-4-ylmethyl)carbamate (7.77 g, 31.3 mmol, Bose, D. Subhas et al., Tetrahedron Lett., 1990, 31, 6903) and 1,6-dioxaspiro[2.5]octane (4.29 g, 37.6 mmol, Satyamurthy, Nagichettiar et al., Phosphorus Sulfur, 1984, 19, 113) in methanol (93 mL) was stirred at room temperature for 20 h. Then the mixture was refluxed for 8 h. After cooling to room temperature, the solvent was removed in vacuo. The residue was chromatographed on a column of silica gel eluting with methanol/dichloromethane (1:20) to give 5.60 g (49%) of the title compound as a colorless oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07776885B2 |
| 출처 데이터셋 | uspto-grants-2010_08 |
| ORD ID | ord-d4f72b04d6c74d59b3097ea0e8ff5696 |
| 출처 메모 | uspto-grants-2010_08 |