참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phthalimide | HCID 6809 | — |
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | Methyl 2-[3-(hydroxymethyl)piperidin-1-yl]benzoate | HCID 58992598 | — |
| 반응물 | Diethylazodicarboxylate toluene | HCID 66777355 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-[[1-[2-(Methoxycarbonyl)phenyl]piperidin-3-yl]methyl]phthalimide | HCID 58992691 | 95% |
반응 단계
Triphenylphosphine (1.68 g, 6.20 mmol) and phthalimide (799 mg, 5.43 mmol) were added to methyl 2-[3-(hydroxymethyl)piperidin-1-yl]benzoate (1.29 g, 5.17 mmol) in tetrahydrofuran (10 mL). The reaction mixture was stirred at room temperature for 10 min and a 40% diethyl azodicarboxylate/toluene solution (3.52 mL, 7.76 mmol) was added. The mixture was then stirred at room temperature for 8 hours. Subsequently, water was added and the mixture was extracted with ethylacetate. The extract was washed with brine, followed by drying over magnesium sulfate and evaporation of the solvent. Purification of the resulting residue by silica gel column chromatography (hexane:ethyl acetate=20:1->5:1) gave 1.85 g (95%) of the desired compound as a pale yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07902367B2 |
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| 출처 데이터셋 | uspto-grants-2011_03 |
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| ORD ID | ord-0cc93c605ff844d78e7a84d99a0d7f4f |
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| 출처 메모 | uspto-grants-2011_03 |
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