HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252211Generated: November 3, 2026
4-Toluenesulfonyl chloride → 1-(p-Nitrobenzyloxycarbonyl)-4-(p-toluenesulfonyloxy)piperidine
https://huagongshe.com/reaction/1252211
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 1-(p-Nitrobenzyloxycarbonyl)-4-hydroxypiperidine | HCID 13292709 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 1-(p-Nitrobenzyloxycarbonyl)-4-(p-toluenesulfonyloxy)piperidine | HCID 13292710 | — |
Reaction Steps
To a solution of 1-(p-nitrobenzyloxycarbonyl)-4-hydroxypiperidine (10.54 g) in dry pyridine (105 ml) was added p-toluenesulfonyl chloride (14.35 g) at 0° C., followed by stirring at 25° C. for 23 hours. The reaction mixture was diluted with water and extracted with diethyl ether-dichloromethane (9:1). The extract was washed successively with saturated aqueous sodium chloride, 1N hydrochloric acid, saturated aqueous sodium chloride and saturated aqueous sodium bicarbonate, dried over anhydrous sodium suflate and evaporated to give 1-(p-nitrobenzyloxycarbonyl)-4-(p-toluenesulfonyloxy)piperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04742052 |
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| Source dataset | uspto-grants-1988_05 |
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| ORD ID | ord-82d664200f304f5ca8b05ea2231f7c20 |
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| Source note | uspto-grants-1988_05 |
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