化工社化工社 化学情報印刷レポート · 研究参考用
Hydrogen Bromide → (2S,3R,4S,5S)-2-bromotetrahydro-2H-thiopyran-3,4,5-triyl triacetate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrogen Bromide | HCID 260 | — |
| 反応物 | 1,2,3,4-tetra-O-acetyl-5-thio-D-xylopyranose | HCID 10991244 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | 1,1-Dichloroethane | HCID 6365 | — |
| 生成物 | (2S,3R,4S,5S)-2-bromotetrahydro-2H-thiopyran-3,4,5-triyl triacetate | HCID 10948230 | 39% |
反応手順
3.50 ml of a 30% solution of hydrobromic acid in glacial acetic acid are added at 10° C. to a solution of 2.10 g (6.3.10-3 mol) of 1,2,3,4-tetra-O-acetyl-5-thio-D-xylopyranose in 10 cm3 of dichloroethane. After 2 to 3 h, the reaction medium is hydrolyzed, washed with a solution of sodium bicarbonate and dried over sodium sulfate (Na2SO4) and the solvent is evaporated off to dryness under reduced pressure. 0.87 g (yield: 39%) of the expected product is obtained after precipitation in ether.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05246961 |
| 出典データセット | uspto-grants-1993_09 |
| ORD ID | ord-826a99c45042499d9978bfa9b6772ca8 |
| 出典メモ | uspto-grants-1993_09 |