Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356227Generated: October 25, 2026

Chloromethyl Methyl Ether → N-ethyl-N-[2-(methoxymethyl)oxyethyl]aniline

https://huagongshe.com/reaction/356227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantHexaneHCID 8058—
Reactant2-(N-ethylanilino)ethanolHCID 62338—
SolventTetrahydrofuranHCID 8028—
ProductN-ethyl-N-[2-(methoxymethyl)oxyethyl]anilineHCID 1894147189%

Reaction Conditions

Temperature0 °C

Reaction Steps

55.7 g (0.34 mol) of N-ethyl-N-(2-hydroxylethyl)aniline was dissolved in 250 ml of anhydrous tetrahydrofuran, and 162 ml (1.2-fold equivalent weight) of a 2.5M hexane solution n-butyllithium was dropwise added thereto over a period of 30 minutes at 0° C. in an atmosphere of argon, followed by stirring at 0° C. for 30 minutes. Next, to the reaction solution obtained, 30.0 g (1.09-fold equivalent weight) of methoxymethyl chloride was dropwise added, and the solution was heated and refluxed for 12 hours, followed by cooling. The precipitate formed was removed by filtration, and thereafter the filtrate obtained was concentrated under reduced pressure. The oily residue thus obtained was distilled under reduced pressure to obtain 63 g of N-ethyl-N-[2-(methoxymethyl)oxyethyl]aniline (yield: 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834575
Source datasetuspto-grants-1998_11
ORD IDord-ace98e2e886e4639a8b04a97b855a07a
Source noteuspto-grants-1998_11