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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069624Generated: October 26, 2026

Methyl iodide → N-methoxy-2-(2-(4-methoxyphenyl)cyclopropyl)-N-methylacetamide

https://huagongshe.com/reaction/2069624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1,2-DimethoxyethaneHCID 8071—
Reactant(E)-N-methoxy-4-(4-methoxyphenyl)-N-methylbut-3-enamideHCID 22347543—
ReactantHCID 178418750HCID 178418750—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-methoxy-2-(2-(4-methoxyphenyl)cyclopropyl)-N-methylacetamideHCID 2234760785.2%

Reaction Steps

The solution of diethyl zinc in hexanes (1M, 17.4 mL, 17.4 mmol) was added slowly to the mixture of iodomethane (2.5 mL, 34.9 mmol), dimethoxy ethane (1.82 mL) in dichloromethane (25 mL) at −15° C. After stifling for 20 minutes, the solution of (E)-N-methoxy-4-(4-methoxyphenyl)-N-methylbut-3-enamide (558) (2.0 g, 8.7 mmol) in dichloromethane (10 mL) was added to the reaction mixture. The resulting mixture was allowed to warm to room temperature over 24 hours. The reaction mixture was diluted with water and extracted with dichloromethane. The organic phase was washed with water, brine, dried over sodium sulfate and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (30% EtOAc in hexanes) to provide N-methoxy-2-(2-(4-methoxyphenyl)cyclopropyl)-N-methylacetamide (559) (1.8 g, 85.2%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299117B2
Source datasetuspto-grants-2012_10
ORD IDord-28b701f7c80b4f83adf5de1e9354c713
Source noteuspto-grants-2012_10