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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1882250Generated: October 31, 2026

Triphenylphosphine → 4-((4-Chloro-2-iodophenoxy)methyl)-1-methylpiperidine

https://huagongshe.com/reaction/1882250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant1-Methyl-4-piperidinemethanolHCID 271971—
Reactant4-Chloro-2-iodophenolHCID 620234—
SolventTetrahydrofuranHCID 8028—
Product4-((4-Chloro-2-iodophenoxy)methyl)-1-methylpiperidineHCID 5888016675%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 4-chloro-2-iodophenol (1.72 g, 6.75 mmol) in anhydrous THF (10.0 mL) were sequentially added (1-methylpiperidin-4-yl)methanol (1.31 g, 10.14 mmol) and triphenyl phosphine (2.66 g, 10.14 mmoL). The reaction mixture was cooled to 0° C., and to it diisopropyl-azodicarboxylate (1.96 mL, 10.14 mmol) was added in drop wise manner. After the addition was over, stirring continued for another 0.5 h at 0° C. and then for 12 h at room temperature. Solvents were removed in vacuum and the residue was purified by silica gel column chromatography, providing Compound 173 (1.85 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318939B2
Source datasetuspto-grants-2012_11
ORD IDord-8bc36d71bd044087a18fd16e66030a89
Source noteuspto-grants-2012_11