참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Chloromethyl Methyl Ether | HCID 7864 | — |
| 반응물 | Hexane | HCID 8058 | — |
| 반응물 | 2-(N-ethylanilino)ethanol | HCID 62338 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-ethyl-N-[2-(methoxymethyl)oxyethyl]aniline | HCID 18941471 | 89% |
반응 단계
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%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05834575 |
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| 출처 데이터셋 | uspto-grants-1998_11 |
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| ORD ID | ord-ace98e2e886e4639a8b04a97b855a07a |
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| 출처 메모 | uspto-grants-1998_11 |
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