Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 264706생성일: 2026년 10월 25일
Sodium Hydroxide → N-{5-(4-Chlorophenyl)pent-1-en-4-yl}-N-ethoxymethyl-3,5-dimethylbenzamide
https://huagongshe.com/reaction/264706
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Chloromethyl ethyl ether | HCID 18523 | — |
| 반응물 | N-{5-(4-chlorophenyl)pent-1-en-4-yl}-3.5-dimethylbenzamide | HCID 19035936 | — |
| 촉매 | Benzyltributylammonium chloride | HCID 159952 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-{5-(4-Chlorophenyl)pent-1-en-4-yl}-N-ethoxymethyl-3,5-dimethylbenzamide | HCID 19035912 | — |
반응 단계
2.36 ml (25.2 mmol) of chloromethyl ethyl ether are added in small portions over the course of 2 hours to a vigorously stirred solution of 5.5 g (16.8 mmol) of N-{5-(4-chlorophenyl)pent-1-en-4-yl}-3.5-dimethylbenzamide and 100 mg of benzyltributylammonium chloride in 15 ml of 50% strength aqueous sodium hydroxide solution and 15 ml of dichloromethane at 0°-5°. The organic phase is taken up in dichloromethane and water, the organic phase is separated off, dried over sodium sulfate and evaporated to dryness under reduced pressure. The oily residue is purified by chromatography on silica gel with ethyl acetate/hexane (1:4) as mobile phase; TLC (ethyl acetate/hexane; 1:3):Rf =0.50; 1H-NMR (300 MHz, CDCl3):mixture of rotamers, δ=7.31-7.18 (m, 4 H), 7.04-6.85 (m, 2.6 H), 6.42 (hr. s, 0.4 H), 5.92-5.60 (m, 1 H), 5.20-5.02 (m, 2 H), 4.54-4.24 (m, 2 H), 3.96-3.67 (m, 1 H), 3.25-2.40 (m, 6 H), 2.28 (s, ca 5 H), 2.24 (s, ca 1 H), 1.34-1.21(m, ca 0.5 H), 1.08 (t, J=7, ca 2.5 H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05646144 |
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| 출처 데이터셋 | uspto-grants-1997_07 |
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| ORD ID | ord-fdce7d4e72c04bffb1204638a1122797 |
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| 출처 메모 | uspto-grants-1997_07 |
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