Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1731094생성일: 2026년 10월 27일
Acetic Anhydride → 4-benzyloxy-3-acetylamino-alpha-[N-benzyl-N-(1-methyl-2-p-hydroxyphenylethyl)aminomethyl] benzyl alcohol
https://huagongshe.com/reaction/1731094
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | 3-amino-4-benzyloxy-alpha-[N-benzyl-N-(1-methyl-2-p-hydroxyphenylethyl)-aminomethyl]benzyl alcohol | HCID 53901474 | — |
| 생성물 | 4-benzyloxy-3-acetylamino-alpha-[N-benzyl-N-(1-methyl-2-p-hydroxyphenylethyl)aminomethyl] benzyl alcohol | HCID 68135822 | — |
반응 단계
In 20 ml. of acetic anhydride there was dissolved 4.0 g. of 3-amino-4-benzyloxy-α-[N-benzyl-N-(1-methyl-2-p-hydroxyphenylethyl)aminomethyl] benzyl alcohol [A] prepared above and after heating the mixture to 65°-80° C for one hour and 30 minutes, the reaction mixture was concentrated under reduced pressure. The residue was dissolved in a mixture of 15 ml. of methanol and 2.0 g. of potassium hydroxide and the solution was stirred for one hour at room temperature. Then, methanol was distilled off under reduced pressure and after water was added to the residue, the residue was extracted with benzene. The extract was washed with water, dried over anhydrous magnesium sulfate, and dried. Thereafter, by distilling off the solvent, 3.8 g. of a crystalline powder of 4-benzyloxy-3-acetylamino-α-[N-benzyl-N-(1-methyl-2-p-hydroxyphenylethyl)aminomethyl] benzyl alcohol [A] was obtained. By recrystallizing 2.0 g. of the product thus obtained from 20 ml. of ethanol 1.6 g. of the crystalline pure product was obtained, melting at 141°-143° C.______________________________________Elemental analysis for C32H36N2O4 : C(%) H(%) N(%)______________________________________Calculated: 75.55 6.92 5.34Found: 75.62 7.03 5.21______________________________________
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US03994974 |
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| 출처 데이터셋 | uspto-grants-1976_11 |
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| ORD ID | ord-a5c4ad90648442e999039b4b247903ea |
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| 출처 메모 | uspto-grants-1976_11 |
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