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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480711Generated: October 31, 2026

Piperidine → 2-(3-((1-Ethoxy-2-methyl-1-oxopropan-2-yl)oxy)phenyl)acetic acid

https://huagongshe.com/reaction/480711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantTriphenylphosphineHCID 11776—
ReactantEthyl 2-[3-(Allyloxycarbonylmethyl)phenoxy]-2-methylpropionateHCID 18766532—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product2-(3-((1-Ethoxy-2-methyl-1-oxopropan-2-yl)oxy)phenyl)acetic acidHCID 18766570—

Reaction Steps

Ethyl 2-[3-(allyloxycarbonylmethyl)phenoxy]-2-methylpropionate (6.40 g, 20.9 mmol) was dissolved in tetrahydrofuran (150 mL). Subsequently, triphenylphosphine (2.42 g, 2.09 mmol) and piperidine (41.34 mL, 41.8 mmol) were added thereto. Under argon atmosphere, tetrakis(triphenylphosphine)palladium (2.42 g, 2.09 mmol) was added, the resultant mixture was stirred for three hours at room temperature. After completion of reaction, the reaction mixture was concentrated under reduced pressure, followed by addition of chloroform and washing sequentially with 3M hydrochloric acid, water, and saturated brine. The resultant mixture was subjected to drying over sodium sulfate, concentration under reduced pressure, and purification by silica gel column chromatography (chloroform/methanol/acetic acid=50/1/0.5), whereby the target compound was obtained (6.88 g, 25.84 mmol, >q.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06653334B1
Source datasetuspto-grants-2003_11
ORD IDord-a16490dc568b4715a8b592f42156dcf5
Source noteuspto-grants-2003_11