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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Reactant | 2-Bromo-m-xylene | HCID 68471 | — |
| Reactant | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Catalyst | (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium | HCID 6505921 | — |
| Product | Ethyl 2-(2,6-dimethylphenyl)acetate | HCID 54752301 | 81% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376417B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-2beb892d8e024c1f890215a6673ba410 |
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| Source note | uspto-grants-2016_06 |
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