戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 848123作成日:2026年10月27日

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

https://huagongshe.com/reaction/848123

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物2-Amino-2'-fluoro-5-nitrobenzophenoneHCID 67657—
反応物N-(Benzyloxycarbonyl)-DL-alanineHCID 95657—
溶媒TetrahydrofuranHCID 8028—
生成物Rac-benzyl-{1-[[2-(o-fluorobenzoyl)-4-nitrophenyl]carbamoyl]ethyl}carbamateHCID 20562333—

反応手順

50 g of carbobenzoxy-DL-alanine are dissolved in 400 ml of absolute tetrahydrofuran, treated dropwise while cooling with ice with 30 g of thionyl chloride and stirred for 40 minutes, a suspension of 50 g of 2-amino-5-nitro-2'-fluorobenzophenone in 200 ml of absolute tetrahydrofuran then being rapidly added dropwise. Subsequently, the mixture is stirred at room temperature for 18 hours, the solution is concentrated and the residue is treated with ice and 10% sodium bicarbonate solution. The mixture is extracted with methylene chloride, the organic solution is dried with sodium sulphate, filtered and concentrated. The residue is crystallised from ethanol and yields rac-benzyl-{1-[[2-(o-fluorobenzoyl)-4-nitrophenyl]carbamoyl]ethyl}-carbamate which is further processed directly as the crude product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04294758
出典データセットuspto-grants-1981_10
ORD IDord-0f98b1f17cf4496c80eac146beee190a
出典メモuspto-grants-1981_10