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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902685Generated: October 30, 2026

Triphenylphosphine → Methyl [3-(3-bromopropoxy)phenyl]acetate

https://huagongshe.com/reaction/902685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant3-Bromo-1-propanolHCID 12308—
ReactantMethyl 3-HydroxyphenylacetateHCID 39129—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
ProductMethyl [3-(3-bromopropoxy)phenyl]acetateHCID 1056518981%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of methyl 3-hydroxyphenylacetate (11.3 g, 0.068 mole) in 300 mL of anhydrous toluene was treated with 3-bromopropanol (12.2 g, 0.088 mole). Polymer bound triphenylphosphine (36.0 g, 0.108 mole, 3 mmol/g, Fluka Chemie) was then added, and the mixture reacted for 15 minutes. The reaction mixture was then cooled to 0° C. and diisopropylazodicarboxylate (16.9 g, 0.084 mol) was added in a dropwise fashion. After stirring at room temperature overnight, the crude reaction mixture was filtered and the solid washed with 100 mL toluene. After concentration of the filtrate in vacuo, the crude product was purified by column chromatography over silica gel (silica gel 60, EM Science) using 15% EtOAc:hexane as eluent to afford 15.8 g (81% yield) of the title compound as an oil:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365085B2
Source datasetuspto-grants-2008_04
ORD IDord-d0620fa9b2174f83a5b9ad52fd872eff
Source noteuspto-grants-2008_04