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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384979Generated: October 31, 2026

Triphenylphosphine → 3-(4-Bromo-2,6-dimethylphenoxymethyl)-1-methylpiperidine

https://huagongshe.com/reaction/1384979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant4-Bromo-2,6-dimethylphenolHCID 16919—
Reactant(1-Methyl-3-piperidyl)methanolHCID 97998—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
SolventTetrahydrofuranHCID 8028—
Product3-(4-Bromo-2,6-dimethylphenoxymethyl)-1-methylpiperidineHCID 994865666.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Hydroxymethyl-1-methylpiperidine (0.4 mL, 3.14 mmol) and triphenylphosphine (1.01 g, 3.85 mmol) were added to a solution of 4-bromo-2,6-dimethylphenol (517 mg, 2.57 mmol) in tetrahydrofuran (10 mL) at 0° C. under dry nitrogen, followed by the dropwise addition of diethyl azodicarboxylate (0.57 mL, 3.60 mmol). The mixture was stirred at 0° C. for 4 hours and the solvent removed in vacuo. The residue was purified on silica gel, eluting with 5% methanol in dichloromethane containing 0.25% ammonium hydroxide, to give 3-(4-bromo-2,6-dimethylphenoxymethyl)-1-methylpiperidine as an oil (531 mg, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262078B1
Source datasetuspto-grants-2001_07
ORD IDord-398eaab2aa0c4960b356c18f8627fb95
Source noteuspto-grants-2001_07