HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623247Generated: October 26, 2026
Pyridine → (4-methoxytetrahydro-2H-pyran-4-yl)methyl 4-methylbenzenesulfonate
https://huagongshe.com/reaction/1623247
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | o-Toluenesulfonyl chloride | HCID 8623 | — |
| Reactant | (4-Methoxyoxan-4-yl)methanol | HCID 66937097 | — |
| Product | (4-methoxytetrahydro-2H-pyran-4-yl)methyl 4-methylbenzenesulfonate | HCID 58127128 | — |
Reaction Steps
To a solution of (4-methoxytetrahydro-2H-pyran-4-yl)methanol (300 mg, 2.05 mmol) in pyridine (4 ml) at ambient temperature was added toluenesulfonic chloride (430 mg, 2.25 mmol) and the resulting mixture was stirred overnight at about 25° C. The stirred mixture was concentrated and the solid residue was dissolved in DCM and purified by silica gel chromatography using a 12 g column, eluting with 0-30% ethyl acetate in heptane to yield the desired compound “O” as a light yellow solid (360 mg). 1H NMR (300 MHz, CHLOROFORM-d) δ ppm 1.45-1.63 (m, 2H) 1.61-1.79 (m, 2H) 2.46 (s, 3H), 3.16 (s, 3H) 3.53-3.75 (m, 4H) 3.93 (s, 2H), 7.36 (d, J=8.20 Hz, 2H) 7.81 (d, J=8.20 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08778951B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-dca7d2b08e84453b85741688eb2ca4ab |
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| Source note | uspto-grants-2014_07 |
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