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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644583Generated: October 25, 2026

Tributylphosphine → Methyl 3-isopropoxy-5-(3-pyridin-3-ylpropoxy)benzoate

https://huagongshe.com/reaction/1644583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant3-PyridinepropanolHCID 17861—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
ReactantMethyl 3-hydroxy-5-isopropoxybenzoateHCID 23072925—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductMethyl 3-isopropoxy-5-(3-pyridin-3-ylpropoxy)benzoateHCID 6677569886.2%

Reaction Steps

To a solution (60 ml) of methyl 5-hydroxy-3-isopropoxybenzoate (2.0 g) and 3-(pyridin-3-yl)propanol (1.6 g) in THF were added successively 1,1′-(azodicarbonyl)dipiperidine (2.9 g) and tributylphosphine (2.8 ml) under ice-cooling, and the mixture was stirred overnight at room temperature. n-Hexane (100 ml) was added to the reaction mixture, and the precipitated crystals were removed by filtration. The filtrate was concentrated under reduced pressure, and the residue was purified by column chromatography (LL, Biotage cartridge, ethyl acetate:n-hexane=15:85→1:4) to give methyl 3-isopropoxy-5-(3-pyridin-3-ylpropoxy)benzoate (2.70 g, 86%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124617B2
Source datasetuspto-grants-2012_02
ORD IDord-1567ed6032804ef2a8faf4a7aa64cbdf
Source noteuspto-grants-2012_02