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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantDiethyl 3-(5-methylpyridin-2-yloxy)benzylphosphonateHCID 86623902—
Catalyst15-Crown-5HCID 36336—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 4-(3-(5-methylpyridin-2-yloxy)benzylidene)piperidine-1-carboxylateHCID 6894843462.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044052B2
Source datasetuspto-grants-2011_10
ORD IDord-c6c147fac8e14cf2acb9712f454e5c8a
Source noteuspto-grants-2011_10