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HRID 1283232作成日:2026年10月26日

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

https://huagongshe.com/reaction/1283232

反応式

関与物質

役割名称HCID仕込み量
反応物4-NitrophenolHCID 980—
反応物BenzyloxycarbonylglycineHCID 14349—
反応物Phosphorous diphenyl esterHCID 426896—
溶媒PyridineHCID 1049—
生成物N-((Phenylmethoxy)carbonyl)glycine 4-nitrophenyl esterHCID 1561675%

反応手順

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 ##SPC6##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03974219
出典データセットuspto-grants-1976_08
ORD IDord-7f0fff29f3874cfb8a398bcae10b0ec3
出典メモuspto-grants-1976_08