関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic acid--water (1/1) | HCID 21899381 | — |
| 反応物 | (S)-di-tert-butyl-5-cyanopyrrolidine-1,2-dicarboxylate | HCID 131734566 | — |
| 触媒 | Hydroxy-nickel | HCID 444642 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | (S)-di-tert-butyl-5-formylpyrrolidine-1,2-dicarboxylate | HCID 131734565 | 51% |
反応手順
90 g Raney-Ni/H2O (50 w % in water, Acros) was added to a solution of 17.905 g (60.42 mmol) of the cyanide 110 in 640 ml Py/AcOH/H2O (2:1:1) and stirred under hydrogen for 72 h at 80° C. 300 ml water was added to the suspension, and the suspension was extracted 3× with 800 ml MTBE each. The combined organic phases were washed twice with water, dried over magnesium sulfate, and the solvent was removed at reduced pressure. The residue was filtered with 1000 ml EtOAc/CyHex (1:1) over silica gel, and, following the removal of the solvent, the raw product was purified by chromatography on silica gel with EtOAc/CyHex 1:4 as eluent. 9.234 g (30.85 mmol, 51%) of the aldehyde 111 was obtained as yellow oil (d.r.: 1.7:1 cis:trans).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09242985B2 |
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| 出典データセット | uspto-grants-2016_01 |
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| ORD ID | ord-4dbdd949243b43deaf76b6a27f3f2494 |
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| 出典メモ | uspto-grants-2016_01 |
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