HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202240Generated: October 30, 2026
Hydrochloric Acid → (S)-(5-Oxotetrahydrofuran-2-yl)methyl 4-methylbenzenesulfonate
https://huagongshe.com/reaction/2202240
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | (S)-(+)-gamma-Hydroxymethyl-gamma-butyrolactone | HCID 2733813 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-(5-Oxotetrahydrofuran-2-yl)methyl 4-methylbenzenesulfonate | HCID 2724793 | 86% |
Reaction Steps
To a solution of (S)-5-(hydroxymethyl)dihydrofuran-2(3H)-one (25.97 g, 223.66 mmol) in THF (125 mL) were added p-toluenesulfonyl chloride (44.8 g, 234.84 mmol), pyridine (45.2 mL, 559.14 mmol) and DMAP (30.1 g, 246.02 mmol) at 0° C., and the mixture was stirred at room temperature for 4 hr. The reaction mixture was poured into ice water (400 mL), and the pH of the mixture was adjusted to 3 with 6N hydrochloric acid. Then, the mixture was extracted with ethyl acetate (×3). The organic layer was washed with water and brine, and dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The crystals were collected by filtration, and washed with IPE/hexane to give (S)-(5-oxotetrahydrofuran-2-yl)methyl 4-methylbenzenesulfonate (51.81 g, 192 mmol, 86%) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09365520B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
|---|
| ORD ID | ord-6ee7beddcc0e478088deddd1b7446c71 |
|---|
| Source note | uspto-grants-2016_06 |
|---|