HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Toluenesulfonyl chloride → (S)-tetrahydrofuran-3-yl 4-methylbenzenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (S)-(+)-3-Hydroxytetrahydrofuran | HCID 2733227 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-tetrahydrofuran-3-yl 4-methylbenzenesulfonate | HCID 13837326 | 90.5% |
Reaction Steps
To a mixture of (S)-tetrahydrofuran-3-ol (1 g, 11.4 mmol) and triethylamine (TEA) (2.3 g, 22.8 mmole) in dichloromethane (DCM) (20 mL) at 0° C. was added 4-methylbenzene-1-sulfonyl chloride (2.2 g, 11.4 mmole). The resulting mixture was stirred at room temperature for 8 h. The mixture was washed with water, dried over MgSO4, filtered, and concentrated. The crude product was purified by ISCO (silica gel, 15% ethyl acetate in hexane) to give the title compound (2.5 g). MS (ESI) m/z: Found: 243.3 (M++1). Calc. 242.3 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08334292B1 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-94d190c2c4764161be3ee30565a5da39 |
| Source note | uspto-grants-2012_12 |