HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649403Generated: October 29, 2026
Pyridine → 5-(1-Benzyloxycarbonyl-4-piperidyl)pentylp-toluenesulfonate
https://huagongshe.com/reaction/649403
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 5-(1-Benzyloxycarbonyl-4-piperidyl)pentanol | HCID 14046930 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-(1-Benzyloxycarbonyl-4-piperidyl)pentylp-toluenesulfonate | HCID 20143653 | — |
Reaction Steps
A mixture of 18 g of 5-(1-benzyloxycarbonyl-4-piperidy)pentanol and 150 ml of pyridine is stirred under ice-cooling, and 14.6 of tosyl chloride is added portionwise to the mixture over the period of 30 minutes. After stirring for another 1 hour under ice-cooling, 2 ml of ice-cold water is added dropwise. Ethyl acetate (500 ml) is added to the reaction solution, which is then washed with 500 ml of 2N-hydrochloric acid and 500 ml of 1N hydrochloric acid successively, further with dilute aqueous sodium hydrogencarbonate solution and water successively, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting oily material is purified by silica-gel column chromatography to give 18 g of 5-(1-benzyloxycarbonyl-4-piperidyl)pentyl p-toluenesulfonate as an oily material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04739066 |
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| Source dataset | uspto-grants-1988_04 |
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| ORD ID | ord-21bf55dc825c438f9e23fff32370ad94 |
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| Source note | uspto-grants-1988_04 |
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