HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980613Generated: October 28, 2026
Pyridine → 5-(1-Benzyloxycarbonyl-4-piperidyl)pentylp-toluenesulfonate
https://huagongshe.com/reaction/980613
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 | 66.5% |
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 g 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 2 N-hydrochloric acid and 500 ml of 1 N hydrochloric acid successively, further with dilute aqueous sodium hydrogen-carbonate 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 | US04638000 |
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| Source dataset | uspto-grants-1987_01 |
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| ORD ID | ord-1cb77232808249c9b566afb7e495d902 |
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| Source note | uspto-grants-1987_01 |
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