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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22178Generated: October 28, 2026

Hydrochloric Acid → 6-ethyl-N,N-dimethyl-2-methoxy-benzamide

https://huagongshe.com/reaction/22178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl BromideHCID 6332—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant2-Methoxy-N,N-dimethylbenzamideHCID 11159646—
ReactantCID 53628100HCID 178418400—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventCyclohexane isopentaneHCID 19019564—
Product6-ethyl-N,N-dimethyl-2-methoxy-benzamideHCID 19927392—

Reaction Conditions

Temperature-70 °C

Reaction Steps

39.5 g of N,N-dimethyl-2-methoxy-benzamide and 28.5 ml of tetramethylethylenediamine are introduced into 190 ml of absolute tetrahydrofuran and the mixture is lithiated at -70° C. with 150 ml of a 1.4-molar sec-butyllithium solution in cyclohexane/isopentane. After subsequently stirring at -70° C. for 45 minutes, 25.6 ml of ethyl bromide are added dropwise within 25 minutes and the reaction mixture is then allowed to warm slowly to room temperature. Water is then added and the mixture is adjusted to pH 2 with hydrochloric acid and extracted twice with diethyl ether. The residue is purified on silica gel using ethyl acetate/n-hexane (4:6) to yield 6-ethyl-N,N-dimethyl-2-methoxy-benzamide in the form of a colourless oil, 1H-NMR (CDCl3): 3.82 ppm (m), 3.40 ppm (m) and 3.12 ppm (2q, N(CH2CH3)2), 2.56 ppm (m, CH2CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428002
Source datasetuspto-grants-1995_06
ORD IDord-e236a500874a40a585bf4dcbacb3eccc
Source noteuspto-grants-1995_06