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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 2-(N-ethylanilino)ethanol | HCID 62338 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-ethyl-N-[2-(methoxymethyl)oxyethyl]aniline | HCID 18941471 | 89% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05834575 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-ace98e2e886e4639a8b04a97b855a07a |
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| Source note | uspto-grants-1998_11 |
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