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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656934Generated: October 30, 2026

Hydrochloric Acid → N-(3,5-difluorophenyl)-3,3-bis(methyloxy)propanamide

https://huagongshe.com/reaction/656934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium ChlorideHCID 25517—
Reactant3,5-DifluoroanilineHCID 96595—
ReactantMethyl 3-methoxyprop-2-enoateHCID 2724617—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
ProductN-(3,5-difluorophenyl)-3,3-bis(methyloxy)propanamideHCID 68811062126%

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of 3,5-difluoroaniline (5 g, 38.8 mmol), methyl-3-methoxyacrylate (4.6 ml, 42.7 mmol) and sodium methoxide solution (25% in MeOH, 12 ml) in toluene (50 ml) under Argon was stirred at 70° C. for 3 h. More sodium methoxide solution (25% in MeOH, 6 mL) added and reaction stirred overnight. Still more sodium methoxide solution (25% in MeOH, 12 mL) and methyl-3-methoxyacrylate (5 mL, 46.4 mmol) were then added and reaction was heated at 70° C. for 5 h. MeOH was added and volume of toluene was reduced to about 10 ml. The residue was acidified to pH 7 using a saturated solution of ammonium chloride, solid ammonium chloride and 5N HCl. The aqueous phase was extracted using ethyl acetate (2×500 ml). The combined organic phases were dried, evaporated and the residue was chromatographed on silica gel, eluting with 0-100% ethyl acetate-40-60° C. petroleum ether to afford the impure desired compound (12 g, 126%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071592B2
Source datasetuspto-grants-2011_12
ORD IDord-896f8d997f37489995025d3895b6ec80
Source noteuspto-grants-2011_12