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Acetic Acid → (R)-2-(Tetrahydropyranyloxy)propionic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | (R)-2-(tetrahydro-pyran-2-yloxy)-propionic acid methyl ester | HCID 11593565 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | (R)-2-(Tetrahydropyranyloxy)propionic acid | HCID 22852535 | 81% |
反応手順
In ethanol (510 ml) was dissolved methyl (2R)-2-(3,4,5,6-tetrahydro-2H-pyran-2-yloxy)propionate (42.7 g), to which was added, under ice-cooling, a 2N solution of sodium hydroxide (170 ml), followed by stirring for one hour at room temperature. The reaction mixture was cooled with ice, to which was added a 26% aqueous solution of acetic acid (120 ml), followed by extraction with dichloromethane (200 ml) three times. Dichloromethane layers were combined, washed with a saturated aqueous sodium chloride solution (100 ml) twice, and dried over anhydrous magnesium sulfate, followed by distilling off the solvent under reduced pressure to leave (2R)-2-(3,4,5,6-tetrahydro-2H-pyran-2-yloxy)propionic acid (32 g) as a colorless waxy product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05405861 |
| 出典データセット | uspto-grants-1995_04 |
| ORD ID | ord-7d18882e100a427eb117b1010d886a12 |
| 出典メモ | uspto-grants-1995_04 |