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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507989Generated: November 2, 2026

2,6-Dimethylphenol → Methyl 4-{[4-(2,6-dimethylphenoxy)piperidin-1-yl]methyl}-3-isopropoxybenzoate

https://huagongshe.com/reaction/507989

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DimethylphenolHCID 11335—
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
ReactantMethyl 4-[(4-hydroxypiperidin-1-yl)methyl]-3-isopropoxybenzoateHCID 23157343—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-{[4-(2,6-dimethylphenoxy)piperidin-1-yl]methyl}-3-isopropoxybenzoateHCID 2315728436.3%

Reaction Steps

To a solution of methyl 4-[(4-hydroxypiperidin-1-yl)methyl]-3-isopropoxybenzoate (0.72 g, 2.34 mmol), 2,6-dimethylphenol (0.43 g, 3.51 mmol) and tributylphosphine (0.88 mL, 3.51 mmol) in anhydrous tetrahydrofuran (14 mL) was added 1,1′-(azodicarbonyl)dipiperidine (0.89 g, 3.51 mmol), and the mixture was stirred at room temperature for 12 hr. To the reaction mixture were added reagents (2,6-dimethylphenol, tributylphosphine and 1,1′-(azodicarbonyl)dipiperidine) in the same amount as mentioned above, and the mixture was further stirred for 12 hr. Diethyl ether (40 mL) was added to the reaction solution, the precipitate was filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=10/1-hexane/ethyl acetate=2/1) to give the title compound (0.35 g, yield 36%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786165B2
Source datasetuspto-grants-2010_08
ORD IDord-09029761993d4faa807ebcd5e9a8491f
Source noteuspto-grants-2010_08