HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282016Generated: October 28, 2026
Diethyl Ether → 1-t-Butoxycarbonyl-4-(2-cyclopentyl-2-hydroxyethyl)piperidine
https://huagongshe.com/reaction/1282016
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Cyclopentanone | HCID 8452 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Tert-butyl 4-(iodomethyl)piperidine-1-carboxylate | HCID 10448961 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Product | 1-t-Butoxycarbonyl-4-(2-cyclopentyl-2-hydroxyethyl)piperidine | HCID 18423503 | — |
Reaction Steps
To a solution of 1.36 g (4.2 mmol) of 1-t-butoxycarbonyl-4-iodomethylpiperidine in 40 mL of ether at −78° C. was carefully added 5.8 mL (9.35 mmol) of t-butyl lithium (1.7 N on pentane). After stirring for 30 min, to the reaction mixture was added dropwise 0.95 mL (10.73 mmol) of cyclopentanone and the reaction mixture was stirred at −78° C. for 2 h. To the reaction mixture was added 5 mL of sat'd NH4Cl solution and the reaction mixture was warmed to rt. The reaction mixture was partitioned between sat'd NH4Cl solution and ether. The aqueous fraction was extracted with ether and the combined organic fractions were washed with sat'd NaCl solution, dried over MgSO4, filtered and the filtrate was concentrated. The residue was purified by chromatography (silica, hexanes:ether, 4:1) to give 0.36 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06455548B2 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-f799b7bf98ca4e61a1c807b9fe88282d |
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| Source note | uspto-grants-2002_09 |
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