HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666405Generated: October 26, 2026
Water → tert-Butyl 4-(3-(5-methylpyridin-2-yloxy)benzylidene)piperidine-1-carboxylate
https://huagongshe.com/reaction/1666405
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Reactant | Diethyl 3-(5-methylpyridin-2-yloxy)benzylphosphonate | HCID 86623902 | — |
| Catalyst | 15-Crown-5 | HCID 36336 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl 4-(3-(5-methylpyridin-2-yloxy)benzylidene)piperidine-1-carboxylate | HCID 68948434 | 62.4% |
Reaction Steps
Diethyl 3-(5-methylpyridin-2-yloxy)benzylphosphonate (1.75 g, 5.22 mmol) from Step 3 and 1,4,7,10,13-pentaoxacyclopentadecane (15-Crown-5, 0.02 mL, 0.10 mmol) were combined in THF (5 mL). Sodium hydride (230 mg, 60% dispersion in mineral oil, 5.74 mmol) was added. The reaction was stirred for 30 min and then a solution of 4-oxo-piperidine-1-carboxylic acid tert-butyl ester (1.14 g, 5.74 mmol) in THF (5 mL) was added. After 16 h, water was added and the layers were separated. The aqueous layer was extracted with EtOAc (2×200 mL) and the combined organic layer was dried over anhydrous sodium sulfate, filtered and concentrated. The residue was purified by silica gel chromatography (0-30%, EtOAc:heptane) to afford the title compound (1.24 g, 62% yield) as a thick oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08044052B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-c6c147fac8e14cf2acb9712f454e5c8a |
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| Source note | uspto-grants-2011_10 |
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