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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666496Generated: October 30, 2026

Water → HCID 66876063, compound

https://huagongshe.com/reaction/1666496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantHCID 86623919HCID 86623919—
Catalyst15-Crown-5HCID 36336—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66876063HCID 6687606335.1%

Reaction Steps

[3-(4-Methyl-pyridin-2-yloxy)-benzyl]-phosphonic acid diethyl ester (2.9 g, 8.6 mmol) from Step 3 and 1,4,7,10,13-pentaoxacyclopentadecane (15-Crown-5, 0.03 mL, 0.17 mmol) were combined in THF (10 mL). Sodium hydride (381 mg, 60% dispersion in mineral oil, 9.51 mmol) was added. The reaction was stirred for 30 minutes and then a solution of 4-oxo-piperidine-1-carboxylic acid tert-butyl ester (1.90 g, 9.51 mmol) in THF (10 mL) was added. After 16 hours, 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 (10-30%, EtOAc:heptane) to afford the desired product (1.15 g, 35% yield) as a thick oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044052B2
Source datasetuspto-grants-2011_10
ORD IDord-f1476becc1fd4d03af4838ae43816e4a
Source noteuspto-grants-2011_10