関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Methyl hydrogen 2-methylenesuccinate | HCID 81791 | — |
| 反応物 | (R)-4-Methoxy-2-methyl-4-oxobutanoic acid | HCID 6398856 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 4-Methoxy-3-methyl-4-oxobutanoic acid | HCID 13925570 | — |
反応手順
133 mg (0.182 mmol) of (RophosARhCOD)CF3SO3 (=precatalyst) were introduced under protective gas into 21 ml of methanol in a 4 l (enamel) Pfaudler autoclave and 526 g (3-65 mol) of 2-methylenesuccinic acid 4-monomethyl ester (=substrate) dissolved in 704 ml of methanol were added. Hydrogenation was then carried out at 40° C. under 5 bar of hydrogen. Conversion of the substrate was complete after 4 h (1H-NMR, 500 MHz). The enantiomeric excess of the product (2R)-methylsuccinic acid 4-monomethyl ester was determined by gas chromatography to be >98% (from: BGB-Analytik, column type: BGB-174, length: 30 m, internal diameter: 0.25 ml, film thickness: 0.25 μm, carrier gas: helium, inlet pressure: 2.35 bar, temperature: 135° C., heating rate: 1.2° C./min, retention time of R enantiomer: 23.3 min, retention time of S enantiomer: 22.6 min). The s/c ratio was 20 000:1.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07557240B2 |
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| 出典データセット | uspto-grants-2009_07 |
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| ORD ID | ord-6800811c6ca04a96994e956cc3e6a28b |
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| 出典メモ | uspto-grants-2009_07 |
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