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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422284Generated: November 1, 2026

Tributylphosphine → HCID 23082820, compound

https://huagongshe.com/reaction/2422284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
ReactantBenzenepropanoic acid, 4-hydroxy-, methyl esterHCID 79706—
Reactant[3-(3-Methylphenoxy)phenyl]methanolHCID 23083121—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
ProductHCID 23082820HCID 2308282055%

Reaction Steps

A solution of methyl 3-(4-hydroxyphenyl)propanoate (0.396 g, 2.20 mmol), [3-(3-methylphenoxy)phenyl]methanol (0.429 g, 2.00 mmol) and tributylphosphine (0.747 mL, 3.00 mmol) in toluene (30 mL) was stirred under ice-cooling, 1,1′-(azodicarbonyl)dipiperidine (0.757 g, 3.00 mmol) was added by small portions, the temperature was raised to room temperature and the mixture was stirred for 18 hrs. Hexane (15 mL) was added to the reaction mixture, the precipitated insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel chromatography (hexane-20% ethyl acetate/hexane) and preparative HPLC (10-95% acetonitrile/water, containing 0.1% trifluoroacetic acid) to give the title compound (0.414 g, yield 55%) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960369B2
Source datasetuspto-grants-2011_06
ORD IDord-d3d33c8b22534448abd0b87696b05cac
Source noteuspto-grants-2011_06