HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256777Generated: October 30, 2026
Diethyl Malonate → Diethyl 2-(3-(2-fluoro-4-biphenylyl)-2-oxobutyl)malonate
https://huagongshe.com/reaction/256777
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Chloro-3-(2-fluoro-4-biphenylyl)-2-butanone | HCID 15676009 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Diethyl 2-(3-(2-fluoro-4-biphenylyl)-2-oxobutyl)malonate | HCID 19785556 | 62% |
Reaction Steps
To a suspension of sodium hydride (1.88 g as 60% in oil, 47.0 mmoles) which was washed with hexane to remove mineral oil and dried, in dimethylformamide (DMF, 23 ml) was added dropwise a solution of diethyl malonate (7.52 g, 47.0 mmoles) in DMF (5 ml) at 0° C. under the stream of nitrogen gas. After elevating the temperature to 50° C., a solution of 1-chloro-3-(2-fluoro-4-biphenylyl)butan-2-one (10.0 g, 36.1 mmoles) in DMF (40 ml) was added dropwise, and the resulting mixture was stirred at the same temperature for 2 hours. The reaction mixture was poured into ice water and extracted with diethyl ether. The organic layer was washed with 1M hydrochloric acid, dried over sodium sulfate and concentrated under reduced pressure. Purification of the residue by medium pressure silica gel column chromatography gave the desired diethyl 2-(3-(2-fluoro-4-biphenylyl)-2-oxobutyl)malonate (8.98 g, 22.4 mmoles, yield 62%) as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05258396 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-3f9b270d60de4f5090a98ca469ea611f |
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| Source note | uspto-grants-1993_11 |
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