Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831824Generated: October 26, 2026

Triphenylphosphine → 4-Chloro-3-[2-(4-chloro-phenyl)-ethoxy]-benzoic acid methyl ester

https://huagongshe.com/reaction/1831824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantp-Chlorophenethylic alcoholHCID 74647—
ReactantDiethyl azodicarboxylateHCID 5462977—
ReactantMethyl 4-chloro-3-hydroxybenzoateHCID 11819787—
SolventTetrahydrofuranHCID 8028—
Product4-Chloro-3-[2-(4-chloro-phenyl)-ethoxy]-benzoic acid methyl esterHCID 69652314—

Reaction Steps

g (5.36 mmol) of 4-Chloro-3-hydroxy-benzoic acid methyl ester was dissolved in 40 ml of anhydrous tetrahydrofuran. To this solution was added 0.923 g (5.9 mmol) of 2-(4-chloro-phenyl)-ethanol, 5.35 g (equivalent to 16.1 mmol PPh3) of triphenylphosphine derivatized polystyrene and 2.80 g (16.1 mmol) of DEAD. The solution was shaken for 16 h at RT. The polymer was filtered off and washed with ethyl acetate. The solvent was removed under reduced pressure. The residue was taken-up in ethyl acetate and the solution was washed three times with water and twice with saturated aqueous sodium chloride. The organic phase was dried with magnesium sulphate, filtered and the solvent was removed under reduced pressure. The residue was chromatographed on silica gel eluting with ethyl acetate/n-heptane (1/5). Yield 1.6 g. LC-MS (ES+): m/e=325 (M)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067665B2
Source datasetuspto-grants-2006_06
ORD IDord-afb5b3f224254532afd1b25dd5f1078d
Source noteuspto-grants-2006_06