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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207133Generated: October 31, 2026

Diethyl Malonate → Ethyl p-tolylacetate

https://huagongshe.com/reaction/2207133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
Reactant4-BromotolueneHCID 7805—
ReactantTetrafluoroboric acidHCID 28118—
Reactant18-Crown-6HCID 28557—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
Catalyst(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
ProductEthyl p-tolylacetateHCID 8417588%

Reaction Conditions

Temperature160 °C

Reaction Steps

A dry Schlenk vessel was initially charged with 171 mg [1 mmol] of 4-bromotoluene, 1056 mg [6.6 mmol] of diethyl malonate, 2.88 mg [0.005 mmol] of Pd(dba)2, 3.19 mg [0.011 mmol] of P(tert-Bu)3×HBF4, 594 mg [2.8 mmol] of dried K3PO4 and 132 mg [0.5 mmol] of 18-crown-6. The reaction vessel was three times evacuated and filled with nitrogen. This was followed by stirring at 160° C. until completion of conversion (8 to 12 hours). After cooling to room temperature, the reaction mixture was diluted with ethyl acetate. The resulting solution was washed successively with 20 ml each of water, saturated aq. NaHCO3 solution and saturated aq. NaCl solution, dried over MgSO4, filtered and concentrated under reduced pressure. Chromatographic purification using silica gel (hexane/ethyl acetate) gave ethyl 4-methylphenylacetate in a yield of 88% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376417B2
Source datasetuspto-grants-2016_06
ORD IDord-320b51359811488a938d0fe09f7ceee9
Source noteuspto-grants-2016_06