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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59901Generated: October 29, 2026

Water → ethyl (R)-6-(3-(2-ethoxyphenoxy)piperidin-1-yl)nicotinate

https://huagongshe.com/reaction/59901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantEthyl 6-chloronicotinateHCID 2799611—
Reactant(R)-3-(2-ethoxyphenoxy)piperidineHCID 42553478—
SolventAcetonitrileHCID 6342—
Productethyl (R)-6-(3-(2-ethoxyphenoxy)piperidin-1-yl)nicotinateHCID 13173707060.9%

Reaction Conditions

Temperature90 °C

Reaction Steps

Triethylamine (8.1 mL, 80 mmol) was added to a stirred solution of (R)-3-(2-ethoxy-phenoxy)-piperidine (10 g, 39 mmol) and ethyl 6-chloronicotinate (7.2 ml, 39 mmol) in acetonitrile (100 mL) at 0° C. The reaction mixture was heated at 90° C. for 16 h. The mixture was cooled to ambient temperature, water (150 mL) was added, and the mixture was extracted with ethyl acetate (3×200 mL). The combined organic layers were washed sequentially with water (100 mL) and brine (100 mL), then were dried over sodium sulfate, filtered and concentrated. The crude material was purified by column chromatography (13% ethyl acetate-hexanes) to afford ethyl (R)-6-(3-(2-ethoxyphenoxy)piperidin-1-yl)nicotinate (8.8 g). MS (ES+) 371.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440949B2
Source datasetuspto-grants-2016_09
ORD IDord-dcb5fc26fcd64ba39881d0c8a6b4c026
Source noteuspto-grants-2016_09