참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dichloromethane | HCID 6344 | — |
| 반응물 | 1-(Bromomethyl)-3-phenoxybenzene | HCID 94544 | — |
| 반응물 | 2-(4-Chlorophenyl)-3-methylbutanamide | HCID 12898176 | — |
| 촉매 | Silver tetrafluoroborate | HCID 159722 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 3-Phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutanimidate | HCID 12898177 | — |
반응 단계
To a refluxing solution of 2.72 g (12.9 mmol) of 2-(4-chlorophenyl)-3-methylbutyramide and 2.27 g (8.6 mmol) of 3-phenoxybenzyl bromide in a solution of 15 ml dichloromethane and 3 ml ethyl ether is added a solution of 1.83 g (9.5 mmol) of silver tetrafluoroborate in ether. The mixture is refluxed for 2 hours and then separated by pouring into ice cold aqueous ethyl acetate/sodium bicarbonate. The organic phase is washed with water, dried and stripped of solvent. The residue is triturated with ether and filtered. The filtrate is concentrated and chromatographed on silica gel, eluting with 25% ethyl acetate/hexane, and then on plates using 35% ethyl acetate/hexane, to yield 3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutanimidate, MS m/e 393 (M+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04254264 |
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| 출처 데이터셋 | uspto-grants-1981_03 |
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| ORD ID | ord-2e3a9f3858cd4cdd9377665e6ee2c8c1 |
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| 출처 메모 | uspto-grants-1981_03 |
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