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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902689Generated: October 25, 2026

Triphenylphosphine → HCID 57757118, compound

https://huagongshe.com/reaction/902689

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—
ProductHCID 57757118HCID 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 mole) in anhydrous toluene (30 mL) was added (S)-(+)-3-bromo-2-methyl-1-propanol (0.90 g, 0.0059 mole). 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, 0.00560 mole) 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 numberUS07365085B2
Source datasetuspto-grants-2008_04
ORD IDord-f951b6c7a1e74b938af9bc909de74fb3
Source noteuspto-grants-2008_04