HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749486Generated: October 26, 2026
Ethyl trimethylsilyl malonate → Ethyl 3-[2,4-dichloro-5-(2-chloro-4,6-difluorophenylamino)phenyl]-3-oxopropionate
https://huagongshe.com/reaction/749486
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl trimethylsilyl malonate | HCID 87655 | — |
| Reactant | 2,4-Dichloro-5-(2-chloro-4,6-difluorophenylamino)benzoyl chloride | HCID 86600258 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 3-[2,4-dichloro-5-(2-chloro-4,6-difluorophenylamino)phenyl]-3-oxopropionate | HCID 68799347 | — |
Reaction Steps
1.4 ml of a 1.6 M solution of butyllithium in hexane was added to a solution of 3.47 g (17.0 mmol) of ethyl trimethylsilyl malonate in 45 ml of diethyl ether at −75° C. in such a way that the temperature did not rise above −60° C. The mixture was then stirred at −75° C. for 30 minutes. The 2,4-dichloro-5-(2-chloro-4,6-difluorophenylamino)benzoyl chloride was dissolved in 45 ml of dimethoxyethane and added dropwise in 40 minutes. The mixture was slowly warmed to 10° C. and stirred at this temperature for 2.5 hours. The reaction mixture was diluted with ethyl acetate and washed twice each with 250 ml portions of water and saturated sodium bicarbonate solution. The organic phase was dried and concentrated. 3.88 g of the crude mixture were obtained and were reacted without further purification in the next stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07402674B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-137ca073d3944f19b6d5b0a457ad8aa8 |
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| Source note | uspto-grants-2008_07 |
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