Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868874Generated: November 1, 2026

Diethyl Malonate → HCID 67099639, compound

https://huagongshe.com/reaction/1868874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
ReactantThionyl ChlorideHCID 24386—
ReactantMagnesium ChlorideHCID 5360315—
ReactantHCID 67099989HCID 67099989—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 67099639HCID 6709963986.9%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 2-(4-chloro-3-fluorophenyl)-2-methylpropanoic acid (2.05 g, 9.46 mmol) in thionyl chloride (40.0 mL, 548 mmol) in a 500 mL round bottom flask was stirred at 95° C. for 2 hours. The reaction was concentrated in vacuo and azeotroped in toluene (50 mL) to give the crude acid chloride. A solution of diethyl malonate (1.43 mL, 9.46 mmol) in ACN (20 mL) was cooled to 0° C. MgCl2 (0.901 g, 9.46 mmol) and then TEA (2.76 mL, 19.9 mmol) were added, and the mixture was stirred at 25° C. for 2 hours. A solution of the acid chloride in ACN (30 mL) was added, and the mixture was stirred at 50° C. for 16 hours. The reaction was cooled, diluted with water (75 mL), and extracted with EtOAc (2×100 mL). The combined organic layers were washed with water (75 mL) and brine (75 mL). The organic layer was dried over MgSO4, concentrated, and dried in vacuo to give diethyl 2-(2-(4-chloro-3-fluorophenyl)-2-methylpropanoyl)malonate (2.95 g). MS m/e=359.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07635715B2
Source datasetuspto-grants-2009_12
ORD IDord-b5b96364249c4ebebc3448415cada714
Source noteuspto-grants-2009_12