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Hydrochloric Acid → 2-Carboxyethyl 2,3,4-tri-O-acetyl-1-thio-beta-L-fucopyranoside
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Propanoic acid, 3-iodo- | HCID 8856 | — |
| 反応物 | 2,3,4-tri-O-acetyl-1-thio-beta-L-fucopyranose | HCID 23238908 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-Carboxyethyl 2,3,4-tri-O-acetyl-1-thio-beta-L-fucopyranoside | HCID 22823286 | 87% |
反応手順
A solution of 2,3,4-tri-O-acetyl-1-thio-β-L-fucopyranose (1.49 g, 4.87 mmol) and freshly crystallized 3-iodopropionic acid (0.97 g, 4.86 mmol) in dichloromethane (20 ml) containing triethylamine (1.35 ml) is kept for 16 hours at room temperature. Hydrochloric acid (2.5 N, 20 ml) and dichloromethane (10 ml) are added and the solution is washed with water, dried, and evaporated in vacuo to a residue that is put on a column of silica gel and eluted with chloroform-methanol-water, 92.5:7.5:0.75 (v/v/v). Compound 23 is isolated in 87% yield (1.6 g), and used, without further purification, for the preparation of 24.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04386026 |
| 出典データセット | uspto-grants-1983_05 |
| ORD ID | ord-112c947c294a458e9cd332d092afcaeb |
| 出典メモ | uspto-grants-1983_05 |