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2-Methylbenzenesulfonic acid → 2-Chloromethyl-4,4,6,6-tetramethyl-1,3-dithiane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Methylbenzenesulfonic acid | HCID 6925 | — |
| 反応物 | 2-Chloro-1,1-dimethoxyethane | HCID 60986 | — |
| 反応物 | 2,4-Dimethyl-2,4-pentanedithiol | HCID 20286103 | — |
| 生成物 | 2-Chloromethyl-4,4,6,6-tetramethyl-1,3-dithiane | HCID 20286123 | — |
反応手順
2-Chloro-1,1-dimethoxyethane (0.1 mole) and 2,4-dimethyl-2,4-pentanedithiol (0.1 mole) are charged into a glass reaction vessel fitted with a mechanical stirrer, thermometer, Dean Stark trap and reflux condenser. Toluene sulfonic acid (0.1 grams) is added and the reaction mixture is heated and thiol removed. When the thiol evolution ceases, the reaction mixture is then cooled to room temperature, treated with sodium carbonate (5 grams) and filtered. Volatiles are stripped from the filtrate using a rotary evaporator to yield the desired product 2-chloromethyl-4,4,6,6-tetramethyl-1,3-dithiane as the residue.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04255182 |
| 出典データセット | uspto-grants-1981_03 |
| ORD ID | ord-1cebef1484be4b479df47b97bc4f2cf4 |
| 出典メモ | uspto-grants-1981_03 |