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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207136Generated: October 29, 2026

Diethyl Malonate → Ethyl 2-(2,6-dimethylphenyl)acetate

https://huagongshe.com/reaction/2207136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
ReactantPotassium CarbonateHCID 11430—
ReactantTetrafluoroboric acidHCID 28118—
Reactant2-Bromo-m-xyleneHCID 68471—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
Catalyst(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
ProductEthyl 2-(2,6-dimethylphenyl)acetateHCID 5475230181%

Reaction Conditions

Temperature160 °C

Reaction Steps

A dry Schlenk vessel was initially charged with 185 mg [1 mmol] of 2,6-dimethylbromobenzene, 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, 207 mg [1.5 mmol] of dried K2CO3 and 150 mg [1.5 mmol] of KHCO3. The reaction vessel was three times evacuated and filled with nitrogen. This was followed by stirring at 160° C. until completion of conversion (8 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 aqueous NaCl solution, dried over MgSO4, filtered and concentrated under reduced pressure. Chromatographic purification using silica gel (hexane/ethyl acetate) gave ethyl 2,6-dimethylphenylacetate in a yield of 81% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376417B2
Source datasetuspto-grants-2016_06
ORD IDord-2beb892d8e024c1f890215a6673ba410
Source noteuspto-grants-2016_06