関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetaldehyde | HCID 177 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 反応物 | 4-(4-Nitrophenyl)piperidine | HCID 15925817 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | HCID 69179394 | HCID 69179394 | — |
反応手順
Sodium triacetoxyborohydride (3.1 g, 14.6 mmol, 3 equiv) is added to a cold (5° C.) solution of 4-(4-nitro-phenyl)-piperidine (1 g, 4.9 mmol) and acetaldehyde (0.82 mL, 14.6 mmol, 3 equiv) in DCM (20 mL). The reaction mixture is stirred for 1 h at 5° C. and then diluted with DCM and a saturated aqueous solution of NaHCO3. The layers are separated and the aqueous layer is extracted with DCM. The organic phase is washed with brine, dried (Na2SO4), filtered and concentrated. The residue is purified by silica gel column chromatography (DCM/MeOH+1% NH3aq, 98:2) to provide the title compound as a yellow oil. ESI-MS: 235.1 [MH]+; tR=2.64 min (purity: 85%, system 1); TLC: Rf=0.14 (DCM/MeOH+1% NH3aq, 98:2).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08759517B2 |
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| 出典データセット | uspto-grants-2014_06 |
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| ORD ID | ord-994abab701f7404d89fd24d4e092ec07 |
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| 出典メモ | uspto-grants-2014_06 |
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