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Hydrochloric Acid → Triethylammonium 1,1,3,3,3-pentafluoro-2-(benzoyloxy)propanesulfonate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Dichloromethane | HCID 6344 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Sodium 2-benzoyloxy-1,1,3,3,3-pentafluoropropanesulfonate | HCID 58112889 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | Triethylammonium 1,1,3,3,3-pentafluoro-2-(benzoyloxy)propanesulfonate | HCID 86618176 | 75% |
反応手順
Triethylamine was dissolved in cold water, and hydrochloric acid was added thereto to adjust the pH of the reaction liquid to fall within a range of 1 to 3. Then sodium 1,1,3,3,3-pentafluoro-2-(benzoyloxy)propanesulfonate and dichloromethane were added thereto and stirred. The separated organic layer was washed with water, and dichloromethane was removed under reduced pressure from the washed organic layer. To the residue thus obtained, diethyl ether was added for recrystallization. The resultant was filtrated and dried to obtain a desired product at a yield of 75%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07871761B2 |
| 出典データセット | uspto-grants-2011_01 |
| ORD ID | ord-9c58d534780a4f299c49d84e8b761102 |
| 出典メモ | uspto-grants-2011_01 |