HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802396Generated: November 2, 2026
4-Toluenesulfonyl chloride → HCID 51900550, compound
https://huagongshe.com/reaction/1802396
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | (2S)-oxan-2-ylmethanol | HCID 6950811 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 51900550 | HCID 51900550 | 77.1% |
Reaction Steps
To a solution of 2.18 g (18.75 mmol) of (2S)-oxan-2-ylmethanol in pyridine (25 mL) are added 7.15 g (37.5 mmol) of p-toluenesulfonylchloride portionwise at 10° C. After complete addition the reaction is allowed to warm to room temperature and stirred for 18 h. The reaction is poured onto a stirred mixture of 6M aqueous HCl/ice. The mixture is extracted with DCM (3×25 mL). The organic layer is dried (MgSO4), filtered and the filtrate is concentrated under reduced pressure to give 3.91 g of (2S)-oxan-2-ylmethyl 4-methylbenzene-1-sulfonate. Yield: 76%, ES-MS: m/z: 293 [M+Na]; 1H NMR (500 MHz, CHLOROFORM-d) δ ppm 1.21-1.32 (1 H, m), 1.41-1.60 (4 H, m), 1.80-1.90 (1 H, m), 2.45 (3 H, s), 3.37 (1 H, td, J=11.41, 2.82 Hz), 3.48-3.58 (1 H, m), 3.89-3.98 (3 H, m), 7.34 (2 H, d, J=8.09 Hz), 7.80 (2 H, d, J=8.24 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08349871B2 |
|---|
| Source dataset | uspto-grants-2013_01 |
|---|
| ORD ID | ord-e33927029aa846c1950d606a728413fc |
|---|
| Source note | uspto-grants-2013_01 |
|---|