HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538629Generated: October 30, 2026
Hydrochloric Acid → (Tetrahydro-2H-pyran-4-yl)methyl 4-methylbenzenesulfonate
https://huagongshe.com/reaction/538629
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Methylcyclohexane | HCID 7962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (Oxan-4-yl)methanol | HCID 2773573 | — |
| Solvent | 2-Methyltetrahydrofuran | HCID 7301 | — |
| Product | (Tetrahydro-2H-pyran-4-yl)methyl 4-methylbenzenesulfonate | HCID 19077576 | 99% |
Reaction Steps
To 97 g (810 mmol) of (tetrahydro-pyran-4-yl)-methanol in 2-methyltetrahydrofuran (190 mL) are added 165 mL of 50% aq. NaOH solution. To this stirred suspension is added dropwise with cooling a solution of p-toluene-sulfonylchloride (283 g, 1.46 mol) in 2-methyltetrahydrofuran (280 mL). The reaction is stirred at 30-35° C. for 18 h. The suspension is poured into a mixture of ice-water (280 mL) and aq. HCl solution (37%, 203 mL). After addition of methylcyclohexane (1.4 L) and further ice-water (0.2 L), the reaction mixture is stirred for 2 h in an ice-bath. The resulting crystalline precipitate is isolated by filtration and washed with methylcyclohexane (0.5 L) and water (0.5 L). Drying under reduced pressure at 40° C. gave 216 g of toluene-4-sulfonic acid tetrahydro-pyran-4-ylmethyl ester. Yield: 99%; ESI-MS: 271 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08865744B1 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-8ea29db611614204bca07ed801ef6bb2 |
|---|
| Source note | uspto-grants-2014_10 |
|---|