HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461024Generated: October 25, 2026
Hydrochloric Acid → Diethyl 3-difluoromethoxy-2,4,5-trifluorobenzoylmalonate
https://huagongshe.com/reaction/1461024
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Magnesium ethanolate | HCID 164963 | — |
| Reactant | 2,4,5-Trifluoro-3-difluoromethoxybenzoyl chloride | HCID 15282971 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Diethyl 3-difluoromethoxy-2,4,5-trifluorobenzoylmalonate | HCID 15023783 | — |
Reaction Steps
Meanwhile, a suspension of diethyl ethoxymagnesium malonate in diethyl ether was prepared from a mixture of 2.80 g (0.0238 moles) of magnesium ethoxide and 3.81 g (0.0238 moles) of diethyl malonate in 60 ml of anhydrous diethyl ether by heating under reflux for 1 hour, whilst stirring. A solution of the 3-difluoromethoxy-2,4,5-trifluorobenzoyl chloride prepared as described above in 50 ml of anhydrous diethyl ether was then added dropwise to the suspension, whilst stirring at room temperature, and the mixture was then stirred at room temperature for an additional 2 hours. 35 ml of 1N aqueous hydrochloric acid were added to the reaction mixture, and the mixture was vigorously stirred. The organic layer was then separated, washed with water and dried over anhydrous sodium sulfate. The solvent was then removed by evaporation under reduced pressure to give 7.07 g of diethyl 3-difluoromethoxy-2,4,5-trifluorobenzoylmalonate [(XIV), R1 =--OCHF2, R3' =H, R17 =C2H5, X=X'=F] as a brown liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05073556 |
|---|
| Source dataset | uspto-grants-1991_12 |
|---|
| ORD ID | ord-7026d0a9ab3049a4a6875258a056522a |
|---|
| Source note | uspto-grants-1991_12 |
|---|