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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656855Generated: October 30, 2026

3-Fluoroaniline → N-(3-fluorophenyl)-3,3-bis(methyloxy)propanamide

https://huagongshe.com/reaction/656855

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-FluoroanilineHCID 9742—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl 3-methoxyacrylateHCID 5323651—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductN-(3-fluorophenyl)-3,3-bis(methyloxy)propanamideHCID 6880959940%

Reaction Conditions

Temperature70 °C

Reaction Steps

3-Fluoroaniline (50 g, 450 mmol) was dissolved in toluene (500 ml) and 25% NaOMe in MeOH (120 ml) and methyl (2E)-3-(methyloxy)-2-propenoate (57.4 ml, 495 mmol) were added. The mixture was then heated to 70° C. and stirred at this temperature for 2.5 hours. The solvent was then reduced to around a quarter of the original volume and the reaction was then treated with NH4Cl until pH 7 was reached (approx 500 ml used). EtOAc was added to the reaction and the layers separated, the aqueous layer was then extracted three times with EtOAc and the combined organic layers dried with MgSO4. The solvents were removed and the crude residues were purified by column chromatography on silica gel using a 30-50% EtOAc/40-60 petroleum ether gradient. Fractions containing product were concentrated to afford the desired compound (40.68 g, 40%) and a less pure batch (6.17 g, 6%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071592B2
Source datasetuspto-grants-2011_12
ORD IDord-99124118a1434b1ca0fe5d9d7fd52d9c
Source noteuspto-grants-2011_12