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HRID 437336作成日:2026年10月26日

Phosphorus pentachloride → Rac-benzyl-{1-[[2-(o-fluorobenzoyl)-4-nitrophenyl]carbamoyl]ethyl}carbamate

https://huagongshe.com/reaction/437336

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphorus pentachlorideHCID 24819—
反応物2-Amino-2'-fluoro-5-nitrobenzophenoneHCID 67657—
反応物N-carbobenzyloxyalanineHCID 736104—
溶媒DichloromethaneHCID 6344—
生成物Rac-benzyl-{1-[[2-(o-fluorobenzoyl)-4-nitrophenyl]carbamoyl]ethyl}carbamateHCID 20562333—

反応条件

温度-40 °C

反応手順

90 g of carbobenzoxy-L-alanine are dissolved in 500 ml of absolute methylene chloride, the solution is cooled to -40° C and treated with 95 g of phosphorus pentachloride. The mixture is stirred at -30° C for 20 minutes and subsequently added to a shaken solution of 52 g of 2-amino-5-nitro-2'-fluorobenzophenone in 250 ml of absolute methylene chloride. The solution is concentrated on a rotary evaporator at 50°-60° C, treated twice with toluene and evaporated each time. By crystallisation of the residue from ether, there is obtained (-)-benzyl-[1-[{2-(o-fluorobenzoyl)-4-nitrophenyl}-carbamoyl]ethyl]carbamate which melts at 158°-160° C and exhibits a rotation of [α]25D =-23.4° (in methylene chloride, 1%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04031078
出典データセットuspto-grants-1977_06
ORD IDord-d4a04a459fb242ab8e26b0f21751110e
出典メモuspto-grants-1977_06