関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Glycerol | HCID 753 | — |
| 反応物 | Methyl bromoacetate | HCID 60984 | — |
| 反応物 | 3-Methylhex-5-en-2-one | HCID 12422318 | — |
| 反応物 | Ammonia chloride | HCID 20976574 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Methyl 3,4-dimethyl-3-hydroxy-6-heptenoate | HCID 86646146 | — |
反応手順
3-Methyl-5-hexen-2-one (J. Chem. Soc., Chem. Comm. 19, 1991, 1399) (17 g, 106 mmol) and methyl bromoacetate (24.4 g, 159 mmol) were dissolved in tetrahydrofuran (100 mL), and the solution was added dropwise to a tetrahydrofuran (50 mL) (zinc (10.4 g, 159 mmol) and trimethyl borate (30 mL)) solution under reflux. After reflux for 3 hours, the mixture was cooled to room temperature, and glycerin (30 mL) and a saturated aqueous solution of ammonia chloride (100 mL) were added thereto, followed by two extractions with ethyl acetate. The ethyl acetate layer was washed with saturated saline, then dried, and then concentrated. The residue was purified by silica gel column chromatography (200 g) to obtain the compound of interest as an oil substance (11.7 g, 60%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07947738B2 |
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| 出典データセット | uspto-grants-2011_05 |
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| ORD ID | ord-915e8305ead74a959ddda63652cb621c |
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| 出典メモ | uspto-grants-2011_05 |
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