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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243071Generated: October 31, 2026

N-Methoxy-N-methylacetamide → HCID 59208500, compound

https://huagongshe.com/reaction/2243071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methoxy-N-methylacetamideHCID 537505—
Reactant1-(2-methoxyethyl)-1H-imidazoleHCID 14366840—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59208500HCID 5920850082.4%

Reaction Steps

A solution of 30 ml (75 mmol) of 2.5 M n-butyllithium in hexanes was added slowly to a solution of 8.48 g (61.3 mmol) 1-(2-methoxyethyl)-1H-imidazole (WO 2003055876 A1) in 200 ml THF cooled in a dry ice-acetone bath. After stirring 1 h, 8 ml (75 mmol) of N-methoxy-N-methylacetamide was added quickly, and the solution was allowed to warm to room temperature over 30 min. After quenching with aqueous NH4Cl, the mixture was diluted with water and extracted twice with EtOAc. The combined EtOAc layers were which washed with brine, dried over anhydrous MgSO4, and concentrated to give an oil that was chromatographed on silica gel (100% DCM followed by gradient elution to 50% EtOAc in DCM). The title compound (8.5 g) was obtained as a mobile oil. MS (ES) (M+H)+: 169 for C8H12CN2O2; NMR: 2.69 (s, 3H), 3.34 (s, 3H), 3.71 (m, 2H), 4.61 (m, 2H), 7.12 (s, 1H), 7.26 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674801B2
Source datasetuspto-grants-2010_03
ORD IDord-4ecdeebc4a054d5c81976a3e356c1542
Source noteuspto-grants-2010_03