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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928080Generated: October 30, 2026

Tert-butyl 3-oxopiperidine-1-carboxylate → Tert-butyl 3-[1-(3-fluorophenyl)methylidene]piperidine-1-carboxylate

https://huagongshe.com/reaction/928080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 3-oxopiperidine-1-carboxylateHCID 2756825—
ReactantPhosphonium, [(3-fluorophenyl)methyl]triphenyl-, bromideHCID 10527583—
ReactantSodium t-butoxideHCID 23676156—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 3-[1-(3-fluorophenyl)methylidene]piperidine-1-carboxylateHCID 8671337548.6%

Reaction Steps

(3-Fluorobenzyltriphenylphosphonium bromide (Intermediate 228, 5.3 g) was added in portions to a solution of sodium tert-butoxide (1.06 g) in anhydrous THF (20 mL) at room temperature and the mixture was stirred for 30 minutes. A solution of tert-butyl 3-oxopiperidine-1-carboxylate (2 g) in anhydrous THF (10 mL) was added dropwise at room temperature and the mixture was stirred for 24 hours. The mixture was diluted with water (100 mL) and extracted with ether (100 mL), washed with brine, dried (Na2SO4) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica eluting with a mixture of ethyl acetate and cyclohexxane with a gradient of 0-20% to give tert-butyl 3-[1-(3-fluorophenyl)-methylidene]piperidine-1-carboxylate (1.42 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290472B2
Source datasetuspto-grants-2016_03
ORD IDord-9b94551b56014567851787861eadf205
Source noteuspto-grants-2016_03