HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → (2S)-2-hydroxy-3,3-dimethylbutyl 4-methylbenzenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | (2S)-3,3-dimethylbutane-1,2-diol | HCID 6951684 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2S)-2-hydroxy-3,3-dimethylbutyl 4-methylbenzenesulfonate | HCID 15692141 | 54.8% |
Reaction Steps
To a solution of (2S)-3,3-dimethyl-butane-1,2-diol (3.1 g, 26.3 mmol) in dichloromethane (25 ml) is added pyridine (4.3 ml, 52.6 mmol). To the mixture is then added dropwise a solution of 4-toluenesulfonyl chloride (5.0 g, 26.3 mmol) in dichloromethane (25 ml) at 0° C. The reaction mixture is warmed to room temperature and stirred for additional 16 h. The reaction mixture is diluted with dichloromethane (50 ml) and washed with 10% copper(II) sulfate solution (2×30 ml). The organic layer is dried over sodium sulfate and evaporated to get the crude product, which is purified by column chromatography (silica gel, 5% ethyl acetate/hexane) affording 4-methyl-benzenesulfonic acid [(2S)-2-hydroxy-3,3-dimethyl-butyl]ester (4.2 g, 14.4 mmol, 54%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09108936B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-381e9629736a4c779c6932e0fac16788 |
| Source note | uspto-grants-2015_08 |