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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156201Generated: October 30, 2026

N-Methylacetamide → N-alpha-methoxyethyl-N-methyl-acetamide

https://huagongshe.com/reaction/1156201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylacetamideHCID 6582—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
Reactant1-Chloro-1-methoxyethaneHCID 137067—
SolventHexaneHCID 8058—
ProductN-alpha-methoxyethyl-N-methyl-acetamideHCID 21464473—

Reaction Steps

First 20 g of triethylamine and then a mixture of 91 g of triethylamine (1.1 moles in total) and 36.5 g (0.5 mole) of N-methylacetamide are added dropwise, at 0° C., to a solution of 94.5 g (1 mole) of α-chloroethyl methyl ether in 200 ml of hexane. After 2 hours, 44 g (1.1 moles) of technical-grade sodium hydroxide flakes are added and 20 ml of 50% strength sodium hydroxide solution are added dropwise, whilst cooling with ice, and the mixture is stirred for a further half an hour. The hexane solution is decanted, the flask is rinsed with hexane and the reaction solution is concentrated, the triethylamine employed being completely recovered in the distillate. The residue is subjected to flash distillation in vacuo. This yields 61 g (93% of theory) of N-α-methoxyethyl-N-methyl-acetamide. Boiling point (23 mm Hg): 84° C. 1H-NMR (CDCl3): 1.2-1.4 ppm (dd); 2.1 ppm (d); 2.8 ppm (d); 3.2 ppm (d); 4.95-5.15 ppm (q); 5.6-5.9 ppm (q).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04334097
Source datasetuspto-grants-1982_06
ORD IDord-0a7d1996f3924a708ee293d020f44955
Source noteuspto-grants-1982_06