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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296968Generated: November 3, 2026

Triphenylphosphine → (S)-[3-(2-Methyl-3-bromopropoxy)phenyl]acetic acid methyl ester

https://huagongshe.com/reaction/1296968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantMethyl 3-HydroxyphenylacetateHCID 39129—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactant(S)-(+)-3-Bromo-2-methyl-1-propanolHCID 10986449—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
Product(S)-[3-(2-Methyl-3-bromopropoxy)phenyl]acetic acid methyl esterHCID 5775711863.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirring solution of (3-hydroxy-phenyl)-acetic acid methyl ester (0.75 g, 0.0045 mol) in anhydrous toluene (30 mL) was added (S)-(+)-3-bromo-2-methyl-1-propanol (0.90 g, 0.0059 mol). Polymer bound triphenylphosphine (2.4 g, 0.0072 mole, 3 mmol/g, Fluka Chemie) was then added, and the mixture was stirred for 15 minutes. The reaction mixture was then cooled to 0° C. and diisopropylazodicarboxylate (1.1 g, 0.0056 mol) was added in a dropwise fashion. After stirring at room temperature overnight, the crude reaction mixture was filtered, and the solid washed with 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 0.86 g (63% yield) of the title compound as an oil: MS (ESI) 303.0 (M+2H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07247748B2
Source datasetuspto-grants-2007_07
ORD IDord-f208aa8f276a4b91ba86875cdb0e9be3
Source noteuspto-grants-2007_07