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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243866Generated: November 2, 2026

Allyl bromide → Methyl 3-(4-(allyloxy)phenyl)-3-(ethoxyimino)propanoate

https://huagongshe.com/reaction/2243866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 3-(ethoxyimino)-3-(4-hydroxyphenyl)propanoateHCID 136360155—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-(4-(allyloxy)phenyl)-3-(ethoxyimino)propanoateHCID 72531910—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of crude methyl 3-(ethoxyimino)-3-(4-hydroxyphenyl)propanoate obtained from Step A at 0° C. was added allyl bromide (0.65 mL) and potassium carbonate (781 mg) in DMF (5 mL), and the resulting suspension was stirred at 0° C. for 2 h. Ethyl acetate and water were added, the aqueous layer was extracted with ethyl acetate (×3), and the combined organic layers were washed with brine, dried over anhydrous sodium sulfate, filtered, and evaporated in vacuo to give the title compound as an oil. The crude product was used in Step C without purification. HPLC retention time: 1.88 min (method A). MS (ESI) (M+H)+ 278.14.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678784B2
Source datasetuspto-grants-2010_03
ORD IDord-12e2caa0a57e4a988e30117271ef2af7
Source noteuspto-grants-2010_03