HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249292Generated: October 25, 2026
Hydrochloric Acid → 2-Chloro-4,5-difluoro-alpha-oxobenzenepropanoic acid ethyl ester
https://huagongshe.com/reaction/249292
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Monoethyl malonate | HCID 70615 | — |
| Reactant | 2-Chloro-4,5-difluorobenzoyl chloride | HCID 10198217 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | 2-Chloro-4,5-difluoro-alpha-oxobenzenepropanoic acid ethyl ester | HCID 53662473 | 87% |
Reaction Steps
Malonic acid monoethyl ester (26 g, 199 mmol) was dissolved in tetrahydrofuran (500 ml) and cooled to -70°. After the addition of n-butyllithium (112.5 ml of a 1.6M solution in hexanes, 180 mmol), the reaction mixture was allowed to warm to -10°, and additional n-butyllithium was added (112.5 ml, as above). The resulting milky-white mixture was cooled to -70°, and treated with 2-chloro-4,5-difluorobenzoyl chloride (19 g, 90 mmol) in tetrahydrofuran (200 ml). After warming to room temperature, the reaction mixture was allowed to stir for an additional 2 hours, then poured into 2N hydrochloric acid (750 ml). The aqueous mixture was extracted with ethyl ether, and the combined organic layers were dried and concentrated to provided the title product as a light amber oil (20.6 g, 78.6 mmol, 87% yield), which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05214051 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-cc154107360447a69a8aee6f0142cf3b |
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| Source note | uspto-grants-1993_05 |
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