HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 4-(2-Fluorophenyl)-3-hydroxy-2-methylbutyl tosylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(2-Fluorophenyl)-3-hydroxy-2-methylbutane-1,3-diol | HCID 22734650 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(2-Fluorophenyl)-3-hydroxy-2-methylbutyl tosylate | HCID 12070574 | 88% |
Reaction Steps
Under a nitrogen atmosphere, a mixture of 13.5 g (68.1 mmol) of 4-(2-fluorophenyl)-3-hydroxy-2-methylbutane-1,3-diol, 14.2 ml (21.3 mmol) of triethylamine, and 70 ml of dichloromethane was cooled with an ice bath and 13.0 g (68.1 mmol) of p-toluenesufonyl chloride was added to the mixture. After stirring overnight at room temperature, 100 ml of water was added thereto, followed by extraction 3 times each with 200 ml of dichloromethane, and the combined organic layer was dried with anhydrous sodium sulfate. After drying, the solvent was distilled off and the residue was purified by silica gel column chromatography to obtain 21.1 g of the title compound as a colorless oil. (Yield: 88%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06717016B2 |
| Source dataset | uspto-grants-2004_04 |
| ORD ID | ord-4e56efa2cda5482fb900e092ba09a00d |
| Source note | uspto-grants-2004_04 |