Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1884264생성일: 2026년 10월 26일
Hydrochloric Acid → N-[2-(4-benzyloxy-3-methoxyphenyl)-1-methylethyl]-3-hydroxy-2-(4-methylphenyl)acrylamide
https://huagongshe.com/reaction/1884264
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | tert-Butoxy bis(dimethylamino)methane | HCID 79885 | — |
| 반응물 | N-[2-(4-benzyloxy-3-methoxyphenyl)-1-methylethyl]-2-(4-methylphenyl)acetamide | HCID 23509014 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-[2-(4-benzyloxy-3-methoxyphenyl)-1-methylethyl]-3-hydroxy-2-(4-methylphenyl)acrylamide | HCID 69900484 | 74% |
반응 단계
2.40 g (5.95 mmol) of N-[2-(4-benzyloxy-3-methoxyphenyl)-1-methylethyl]-2-(4-methylphenyl)acetamide and 3.10 g (17.8 mmol) of t-butoxybis(dimethylamino) methane were mixed and stirred at 80° C. for 2 hours. The reaction mixture was cooled and tetrahydrofuran was added thereto. The reaction mixture was acidified with hydrochloric acid and stirred at room temperature for 2 hours. After the solvent was distilled off under reduced pressure, the residue was extracted with chloroform washed with saturated brine twice, dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was subjected to silica gel chromatography (eluent, hexane:ethyl acetate=3:2) and dried to give 1.90 g of N-[2-(4-benzyloxy-3-methoxyphenyl)-1-methylethyl]-3-hydroxy-2-(4-methylphenyl)acrylamide.
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-3d3def96f8e04ab6ad88fa043a553c78 |
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| 출처 메모 | uspto-grants-2004_07 |
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