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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509221Generated: October 25, 2026

Diethyl Malonate → Ethyl p-tolylacetate

https://huagongshe.com/reaction/509221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
Reactant4-BromotolueneHCID 7805—
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 8417576%

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, 2.22 mg [0.011 mmol] of P(tert-Bu)3, 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 76% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096568B2
Source datasetuspto-grants-2015_08
ORD IDord-5c834350e6a94f7ba204f15f7f26f7ed
Source noteuspto-grants-2015_08