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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1439412생성일: 2026년 10월 27일

4-Nitrophenol → N-((Phenylmethoxy)carbonyl)glycine 4-nitrophenyl ester

https://huagongshe.com/reaction/1439412

반응식

참여 물질

역할이름HCID투입량
반응물4-NitrophenolHCID 980—
반응물BenzyloxycarbonylglycineHCID 14349—
반응물Phosphorous diphenyl esterHCID 426896—
용매PyridineHCID 1049—
생성물N-((Phenylmethoxy)carbonyl)glycine 4-nitrophenyl esterHCID 1561675%

반응 단계

A mixture of 2.93 g. (0.0125 mole) of phosphorous diphenyl ester and 3.37 g. (0.0125 mole) of mercuric chloride was refluxed for 1 hour in 20 ml. of pyridine. Thereafter, 1.74 g. (0.0125 mole) of p-nitrophenol and 10 ml. of pyridine were added, and the mixture was further reacted for 1 hour. To the reaction mixture were added 2.61 g. (0.0125 mole) of Z-Gly.OH having an amino group protected with Z and 10 ml. of pyridine, and the mixture was reacted under reflux for 1 hour. After completion of the reaction, pyridine was removed by distillation under reduced pressure, and the residue was extracted with 100 ml. of ethyl acetate. The ethyl acetate layer was washed with 2N-HCl, a saturated aqueous NaHCO3 solution and water in this order and then dried over anhydrous Na2SO4, and thereafter ethyl acetate was removed by distillation under reduced pressure. The resulting residue was allowed to stand to form a solid, which was then recrystallized from ethanol to obtain N-benzyloxycarbonyl glycine p-nitrophenyl ester (hereinafter represented by ##STR9## in a yield of 75% (3.0 g.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04059603
출처 데이터셋uspto-grants-1977_11
ORD IDord-fcb33f8a7272428888da4fd338b05ff6
출처 메모uspto-grants-1977_11