Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1884263생성일: 2026년 10월 25일
Tetrahydrofuran → N-[2-(4-benzyloxy-3-methoxyphenyl)-1-methylethyl]-2-(4-methylphenyl)acetamide
https://huagongshe.com/reaction/1884263
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 2-(4-Methylphenyl)acetyl chloride | HCID 2760634 | — |
| 반응물 | 3-Methoxy-4-phenylmethoxyphenylisopropylamine | HCID 14579452 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | N-[2-(4-benzyloxy-3-methoxyphenyl)-1-methylethyl]-2-(4-methylphenyl)acetamide | HCID 23509014 | 70.1% |
반응 단계
2.30 g (8.48 mmol) of crude 2-(4-benzyloxy-3-methoxyphenyl)-1-methylethylamine, 1.03 g (10.2 mmol) of triethylamine and 25 ml of tetrahydrofuran were mixed and cooled to about 0° C. and then 1.42 g (8.48 mmol) of (4-methylphenyl)acetyl chloride was added dropwise thereto. The mixture was stirred at 0° C. for 30 minutes and further at room temperature for 2 hours. Water was added to the reaction mixture, which was followed by extracted with ethyl acetate, washed with 5% hydrochloric acid and saturated brine subsequently, dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was washed with hexane and dried to give 2.40 g of N-[2-(4-benzyloxy-3-methoxyphenyl)-1-methylethyl]-2-(4-methylphenyl) acetamide.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06762321B2 |
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| 출처 데이터셋 | uspto-grants-2004_07 |
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| ORD ID | ord-2db66898ab8045e3b068d5d260c468c6 |
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| 출처 메모 | uspto-grants-2004_07 |
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