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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2922Generated: October 27, 2026

Water → N-(2,6-dimethoxy-4-methylphenyl)isovaleramide

https://huagongshe.com/reaction/2922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantIsovaleryl chlorideHCID 66054—
Reactant2,6-Dimethoxy-4-methylanilineHCID 12409090—
SolventDiethyl EtherHCID 3283—
ProductN-(2,6-dimethoxy-4-methylphenyl)isovaleramideHCID 1893649292%

Reaction Conditions

Temperature0 °C

Reaction Steps

8.2 g of 2,6-dimethoxy-4-methylaniline are dissolved in 100 ml of diethyl ether at 0° C. under an inert atmosphere, 5.96 g of triethylamine are added to the reaction mixture and then 6.51 g of isovaleryl chloride are added dropwise, while maintaining the temperature at 0° C. The mixture is left at room temperature for 30 minutes and is then poured into 250 ml of water. The aqueous phase is extracted with ethyl acetate after separation by settling of the ethereal phase. The organic phases are combined and washed with water, then dried over anhydrous sodium sulphate and evaporated to dryness. The white crystals of N-(2,6-dimethoxy-4-methylphenyl)isovaleramide obtained are washed with diisopropyl ether; M.p.=139° C., Yield: 92%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05731340
Source datasetuspto-grants-1998_03
ORD IDord-008f672ce81f498d931758715cd6380b
Source noteuspto-grants-1998_03