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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

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물3-amino-4-benzyloxy-alpha-[N-benzyl-N-(1-methyl-2-p-hydroxyphenylethyl)-aminomethyl]benzyl alcoholHCID 53901474—
생성물4-benzyloxy-3-acetylamino-alpha-[N-benzyl-N-(1-methyl-2-p-hydroxyphenylethyl)aminomethyl] benzyl alcoholHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03994974
출처 데이터셋uspto-grants-1976_11
ORD IDord-a5c4ad90648442e999039b4b247903ea
출처 메모uspto-grants-1976_11