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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
ReactantSodium hydrideHCID 24758—
Reactant1-Chloro-3-(2-fluoro-4-biphenylyl)-2-butanoneHCID 15676009—
SolventDimethylformamideHCID 6228—
ProductDiethyl 2-(3-(2-fluoro-4-biphenylyl)-2-oxobutyl)malonateHCID 1978555662%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05258396
Source datasetuspto-grants-1993_11
ORD IDord-3f9b270d60de4f5090a98ca469ea611f
Source noteuspto-grants-1993_11