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Hydrochloric Acid → 3-Bromo-2-methyl-6-methylsulfonylbenzaldehyde
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Formaldehyde | HCID 712 | — |
| 反応物 | Water | HCID 962 | — |
| 反応物 | 3-Bromo-2-methyl-6-methylsulfonylbenzaldoxime | HCID 73461944 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 3-Bromo-2-methyl-6-methylsulfonylbenzaldehyde | HCID 18757277 | — |
反応手順
7.1 g of 3-bromo-2-methyl-6-methylsulfonylbenzaldoxime (23 mmol) are stirred at 65° C. in a mixture of 17 g of 5% strength hydrochloric acid, 2 g of 37% strength formaldehyde solution, 15 ml of water and 30 ml of tetrahydrofuran for 32 hours. During this time, a further 3.5 g of 37% strength formaldehyde solution are added in portions of 0.5 g. The mixture is then cooled to room temperature and the product is filtered off with suction. This gives 5.1 g (79%) of product, purity 94% (according to GC).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06608209B2 |
| 出典データセット | uspto-grants-2003_08 |
| ORD ID | ord-76064d8b8eda456c8ac0bb2f9dc1def2 |
| 出典メモ | uspto-grants-2003_08 |