関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetone | HCID 180 | — |
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Antimony pentachloride | HCID 24294 | — |
| 反応物 | (2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal | HCID 3037556 | — |
| 生成物 | 1,2:3,4-Di-O-isopropylidene-alpha-D-galactopyranose | HCID 2723629 | 82.9% |
反応手順
To 200 ml of acetone were added 10.0 g of D-galactose and 89.7 mg of antimony pentachloride, and the mixture was refluxed with stirring in a water bath of 60° C. for 8 hours. During this reaction, the refluxing solvent was dried with 20 g of Molecular Sieves 3A interposed between the reaction vessel and the condenser. After completion of the reaction, a small amount of pyridine was added to the reaction mixture, and the acetone was distilled off under reduced pressure. The residue was dissolved in benzene, and the solution was washed with aqueous sodium bicarbonate and water, and dried over anhydrous magnesium sulfate. The benzene was distilled off, and the resulting residue was distilled under reduced pressure to give 11.97 g (82.9%) of 1,2:3,4-di-O-isopropylidene-α-D-galactopyranose as a fraction having a boiling point of 129°-133° C./0.2 mmHg.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04659809 |
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| 出典データセット | uspto-grants-1987_04 |
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| ORD ID | ord-47c4bc940fa54da495d155797d5e485e |
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| 出典メモ | uspto-grants-1987_04 |
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