HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440101Generated: October 30, 2026
Hydrochloric Acid → Diethyl (3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoyl)malonate
https://huagongshe.com/reaction/1440101
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 3-Difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoyl chloride | HCID 15023842 | — |
| Product | Diethyl (3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoyl)malonate | HCID 15282967 | — |
Reaction Steps
The whole of the 3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoyl chloride [(XIII), R1 =--OCHF2, R3' =NO2, X=X'=F] prepared as described above was dissolved in 150 ml of anhydrous diethyl ether, and this solution was added dropwise, with stirring at room temperature, to the suspension of diethyl ethoxymagnesium malonate. The resulting mixture was then stirred at room temperature for an additional 2 hours. At the end of this time, 100 ml of 1N aqueous hydrochloric acid were added to the reaction mixture, and, after the mixture had been vigorously stirred, the organic layer was separated, washed with water and dried over anhydrous sodium sulfate. The solvent was then removed by evaporation under reduced pressure to give 31.2 g of diethyl (3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoyl)malonate [(XIV), R1 =--OCHF2, R3' =NO2, R17 =C2H5, X=X'=F] as a red liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05496951 |
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| Source dataset | uspto-grants-1996_03 |
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| ORD ID | ord-f13a89b19c454a10a14283d812fe9d6b |
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| Source note | uspto-grants-1996_03 |
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