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Methanesulfonyl chloride → 3,4,5-Trimethoxybenzyl Mesylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | 3,4,5-Trimethoxybenzyl alcohol | HCID 77449 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 3,4,5-Trimethoxybenzyl Mesylate | HCID 18464591 | — |
反応手順
Combine 3,4,5-trimethoxy-benzyl alcohol (9.0 g, 45.4 mmol), diisopropylethylamine (12.9 g, 100 mmol), and acetonitrile (60 mL). Cool in an ice bath. Add methanesulfonyl chloride (6.76 , 49.0 mmol). After 2 hours, partition the reaction mixture between water and ethyl acetate. Separate the layers and extract the organic layer with 1 M hydrochloric acid solution and them a saturated solution of sodium bicarbonate. Dry the organic layer over Na2SO4, filter, and evaporate in vacuo to give the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06329392B1 |
| 出典データセット | uspto-grants-2001_12 |
| ORD ID | ord-87018fd455e044e9a2f30a01c3ae272a |
| 出典メモ | uspto-grants-2001_12 |