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Benzaldehyde → alpha-L-mannopyranose
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzaldehyde | HCID 240 | — |
| 反応物 | Benzoic Acid | HCID 243 | — |
| 反応物 | Water | HCID 962 | — |
| 反応物 | L-mannose phenylhydrazone | HCID 86737045 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | alpha-L-mannopyranose | HCID 6971016 | — |
反応手順
The hydrazone (20 g.) was then refluxed for 3 hours with a solution containing water (200 ml.), ethanol (40 ml.), benzaldehyde (25 ml.) and benzoic acid (2.5 g.). The solution was cooled and then decanted from benzaldehyde phenylhydrazone, extracted three times with chloroform, decolorized with carbon and concentrated at reduced pressure. The resulting syrup was further evaporated with several portions of absolute ethanol to remove residual water and the resulting syrup (10 g.) was left to crystallize. The crystals were filtered with ethanol to give α-L-mannopyranose, m.p. 125°-126°, [α]D -26.9°→-14.4° (24 hr., c 2.0, water) compared to m.p. 128°-132°, [α]D -14.5° (equilibrium, c 3.4, water).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04207413 |
| 出典データセット | uspto-grants-1980_06 |
| ORD ID | ord-53d58275665e4f8ea062e31255bab0d8 |
| 出典メモ | uspto-grants-1980_06 |