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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 405666Generated: October 29, 2026

Methacrylic Acid → HCID 66795860, compound

https://huagongshe.com/reaction/405666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethacrylic AcidHCID 4093—
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 60199172HCID 60199172—
CatalystPotassium IodideHCID 4875—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 66795860HCID 6679586072%

Reaction Conditions

Temperature25 °C

Reaction Steps

In a four-necked flask with a volume of 500 mL, which was equipped with a thermometer, a stirrer, a dropping funnel, and a nitrogen introducing tube, 9.7 g (70 mmol) of potassium carbonate, 0.7 g (4 mmol) of potassium iodide, 100 mL of dimethylformamide, 25.8 g (300 mmol) of methacrylic acid, and 18.8 g (100 mmol) of 6-chloroacetyl-6-azabicyclo[3.2.0]heptan-7-one obtained in Synthesis Example 3 were charged, and the mixture was stirred at an internal temperature of 25° C. for 5 hours. To the reaction mixture, 100 mL of ethyl acetate and 50 mL of water were added, and a liquid separation operation was then carried out. The obtained organic layer was concentrated under reduced pressure and then purified by means of silica gel column chromatography, thereby obtaining 17.1 g (72 mmol) of 6-methacryloyloxyacetyl-6-azabicyclo[3.2.0]heptan-7-one having the following properties.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08753794B2
Source datasetuspto-grants-2014_06
ORD IDord-3524aa06c7334579bf7bc7b73d1001a3
Source noteuspto-grants-2014_06