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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909536Generated: October 26, 2026

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

https://huagongshe.com/reaction/1909536

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 numberUS08598374B2
Source datasetuspto-grants-2013_12
ORD IDord-afde8469aaa846728dc53118c6184f07
Source noteuspto-grants-2013_12