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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836769Generated: October 29, 2026

Hydrochloric Acid → N-Methoxy-N-methyl-2-phenyl-isobutyramide

https://huagongshe.com/reaction/1836769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Phenylisobutyric acidHCID 13222—
ReactantThionyl ChlorideHCID 24386—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Solventtert-Butyl methyl etherHCID 15413—
ProductN-Methoxy-N-methyl-2-phenyl-isobutyramideHCID 5978866195.2%

Reaction Steps

Dissolve 2-methyl-2-phenyl-propionic acid (15.0 g, 91.2 mmol) in toluene (80 mL) and add, by dropwise addition over 5 minutes, thionyl chloride (15 mL, 206 mmol). Stir at room temperature overnight; add additional thionyl chloride (3 mL, 41.1 mmol) and heat to reflux for 1 hour. Remove excess thionyl chloride by azeotropic distillation with toluene (400 mL). Add toluene (20 mL) to the reaction mixture along with a solution of potassium carbonate (28.0 g, 203 mmol) in water (40 mL). Add, by dropwise addition, a solution of N,O-dimethylhydroxylamine hydrochloride (8.9 g, 91.2 mmol) in water (20 mL) without cooling and stir for 2 hours. Add tert-butylmethyl ether (75 mL) following by slow addition of aqueous HCl (2N, 75 mL) with vigorous stirring. Separate the organic layer and wash with aqueous HCl (2N, 75 mL), saturated hydrogen carbonate (25 mL) and brine (50 mL). Dry the organic layer over (Na2SO4), filter, evaporate the filtrate in vacuo and purify by vacuum distillation to give 2-methyl-2-phenyl-propionic acid, N-methoxy-N-methylamide (18.0 g, 95%); bp 91-103° C/5 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777555B2
Source datasetuspto-grants-2004_08
ORD IDord-4348db74ab664981a349676cf45eeb23
Source noteuspto-grants-2004_08