HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368889Generated: October 31, 2026
Hydrochloric Acid → 1-[(Benzyloxy)carbonyl]-4-hydroxypiperidine-4-carboxylic acid
https://huagongshe.com/reaction/1368889
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | 4-hydroxypiperidine-4-carboxylic Acid | HCID 4437198 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 1-[(Benzyloxy)carbonyl]-4-hydroxypiperidine-4-carboxylic acid | HCID 20394185 | — |
Reaction Steps
The crude 4-hydroxypiperidine-4-carboxylic acid obtained in the above step (a) was dissolved in a mixed solvent of 1 N aqueous sodium hydroxide (1.4 ml) and tetrahydrofuran (2 ml), and the solution was added with benzyl chloroformate (0.1 ml). The reaction mixture was stirred at room temperature for 2 hours and 30 minutes, and then acidified with hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, and the solvent was evaporated to obtain crude 1-benzyloxycarbonyl-4-hydroxypiperidine-4-carboxylic acid. This crude 1-benzyloxycarbonyl-4-hydroxypiperidine-4-carboxylic acid was subjected to the measurement of molecular weight and then used in the following reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06576627B1 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-227b2a08a97642c58ad6cdd9f6e0c442 |
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| Source note | uspto-grants-2003_06 |
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