関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Benzyl chloroformate | HCID 10387 | — |
| 反応物 | D-Glutamic Acid | HCID 23327 | — |
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | Potassium Bicarbonate | HCID 516893 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | Dimethyl (2R)-2-{[(benzyloxy)carbonyl]amino}pentanedioate | HCID 86606597 | — |
反応手順
Thionyl chloride (30 ml) was added to a cooled solution of D-glutamic acid (33.2 g) in methanol (250 ml) and the mixture subsequently heated under reflux for 16 h. On cooling, the mixture was concentrated under reduced pressure and the residue azeotroped with toluene to give a white solid. This was stirred with ethyl acetate, water and potassium hydrogen carbonate at 0° C. while benzyl chloroformate (30 ml) was added. The mixture was warmed to room temperature and stirred for 5 h. The separated organic phase was washed with water, dried (over magnesium sulphate) and concentrated under reduced pressure to provide a yellow oil. This oil was purified using flash column chromatography (silica, eluting with cyclohexane:ethyl acetate 2:1) to give the title compound (22.45 g) as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07084139B2 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-0d66f2913bdf4cf684ad6583f5f27c4b |
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| 出典メモ | uspto-grants-2006_08 |
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