HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615393Generated: November 2, 2026
Water → Ethyl 4-(4-(benzyloxycarbonylamino)piperidin-1-yl)benzoate
https://huagongshe.com/reaction/1615393
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Ethyl 4-(4-aminopiperidin-1-yl)benzoate | HCID 22557718 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 4-(4-(benzyloxycarbonylamino)piperidin-1-yl)benzoate | HCID 66691942 | — |
Reaction Steps
The 4-(4-aminopiperidin-1-yl)-benzoic acid ethyl ester (15.7 g, 63.2 mmol) obtained in Example 7(1) was dissolved in THF (200 ml), and a 2M sodium carbonate aqueous solution (63 ml) was added thereto. Subsequently, benzyloxycarbonyl chloride (11.7 ml, 82.2 mmol) was added thereto, followed by stirring at room temperature for 2 hours. Water was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was washed with water and saturated sodium chloride, and then dried over anhydrous sodium sulfate. After the desiccant was filtered off, the solid obtained by evaporation under reduced pressure was collected by filtration and dried under reduced pressure, thereby obtaining 4-(4-benzyloxycarbonylaminopiperidin-1-yl)-benzoic acid ethyl ester (18.0 g, 74%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765750B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-feb08f97bd674ff7bcfd344a649b6494 |
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| Source note | uspto-grants-2014_07 |
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