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Benzoyl Peroxide → 4-[(6-Acetoxyhexyl)sulfonyl]benzyl bromide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzoyl Peroxide | HCID 7187 | — |
| 反応物 | N-bromobutanimide | HCID 67184 | — |
| 反応物 | 4-[(6-Acetoxyhexyl)sulfonyl]toluene | HCID 18680025 | — |
| 溶媒 | Carbon tetrafluoride | HCID 6393 | — |
| 生成物 | 4-[(6-Acetoxyhexyl)sulfonyl]benzyl bromide | HCID 18680021 | 71% |
反応手順
2.0 g of 4-[(6-acetoxyhexyl)sulfonyl]toluene, 1.3 g of N-bromo-succinimide (NBS), 0.015 g of benzoyl peroxide (BPO) , and 20 mL of carbon tetrafluoride were added to a 250 mL round bottomed flask and heated with reflux for 12 hours in nitrogen. The mixture was allowed to cool down and then filtered. The filtrate was washed by deionized water repeatedly. The organic fraction was dried over anhydrous magnesium sulfate and then concentrated by a rotary evaporator. The concentrate was further purified by re-crystallization to produce a white solid. The yield was 71% with the following structure.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06503998B2 |
| 出典データセット | uspto-grants-2003_01 |
| ORD ID | ord-d625cb0354ea4fdb9c0c5ba8db793974 |
| 出典メモ | uspto-grants-2003_01 |