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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713200Generated: October 26, 2026

Triphenylphosphine → Tert-butyl 4-(2-fluoro-4-methoxyphenoxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/713200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
Reactant2-Fluoro-4-methoxyphenolHCID 2774557—
ReactantDiethyl azodicarboxylateHCID 5462977—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 4-(2-fluoro-4-methoxyphenoxy)piperidine-1-carboxylateHCID 11815928385.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of tert-butyl 4-hydroxypiperidine-1-carboxylate (2.496 g, 12.03 mmol) in THF (33.4 mL) at room temperature was treated with 2-fluoro-4-methoxyphenol (1.181 mL, 10.03 mmol) and triphenylphosphine (3.16 g, 12.03 mmol). The reaction mixture was cooled to 0° C. and DEAD (40 wt % in toluene, 5.95 mL, 15.04 mmol) was added dropwise via syringe. The resulting reaction mixture was stirred at 65° C. for 5 h, then at room temperature overnight. Flash silica gel chromatography using a gradient of 10% to 100% EtOAc in hexanes gave tert-butyl 4-(2-fluoro-4-methoxyphenoxy)piperidine-1-carboxylate (2.78 g, 85%) as a light yellow oil. ESI-MS m/z [M+Na]+ 348.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181249B2
Source datasetuspto-grants-2015_11
ORD IDord-718ccccbb3fc46688fe263456233797a
Source noteuspto-grants-2015_11