HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282240Generated: October 26, 2026
4-Toluenesulfonyl chloride → (4E)-5-(3-Pyridyl)-4-pentene-2-ol p-Toluenesulfonate
https://huagongshe.com/reaction/1282240
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | (4E)-5-(3-Pyridyl)-4-penten-2-ol | HCID 12042974 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | (4E)-5-(3-Pyridyl)-4-pentene-2-ol p-Toluenesulfonate | HCID 87466987 | 60.1% |
Reaction Steps
To a stirred solution of (4E)-5-(3-pyridyl)-4-penten-2-ol (5.00 g, 30.67 mmol) in dry pyridine (30 mL) at 0° C. was added p-toluenesulfonyl chloride (8.77 g, 46.01 mmol). The reaction mixture was stirred for 24 h at ambient temperature. The pyridine was removed by rotary evaporation. Toluene (50 mL) was added to the residue and subsequently removed by rotary evaporation. The crude product was stirred with a saturated solution of sodium bicarbonate (100 mL) and extracted with chloroform (3×100 mL). The combined chloroform extracts were dried over sodium sulfate, filtered, and concentrated by rotary evaporation. The crude product was purified by column chromatography over aluminum oxide, eluting with ethyl acetate-hexane (3:7, v/v). Selected fractions were combined and concentrated by rotary evaporation to give a viscous, brown oil (5.83 g, 60.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06455554B1 |
|---|
| Source dataset | uspto-grants-2002_09 |
|---|
| ORD ID | ord-2720ee4c4c7b427abb67752a93ad1b58 |
|---|
| Source note | uspto-grants-2002_09 |
|---|