戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1278493作成日:2026年10月26日

Thionyl Chloride → Benzyl-rac-{1-[[2-(o-fluorobenzoyl)-4-nitrophenyl]carbamoyl]butyl}carbamate

https://huagongshe.com/reaction/1278493

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-[(Benzyloxy)carbonyl]norleucineHCID 263476—
反応物Sodium BicarbonateHCID 516892—
溶媒TetrahydrofuranHCID 8028—
生成物Benzyl-rac-{1-[[2-(o-fluorobenzoyl)-4-nitrophenyl]carbamoyl]butyl}carbamateHCID 131712305—

反応手順

19.7 g of N-carbobenzoxy-DL-norleucine are dissolved in 200 ml of absolute tetrahydrofuran, the solution is treated dropwise while cooling with ice with 10 g of thionyl chloride and then stirred for 1 hour. To this solution there is rapidly added dropwise a solution of 17 g (0.065 L M) of 2-amino-5-nitro-2'-fluorobenzophenone in 130 ml of absolute tetrahydrofuran and the mixture is then stirred at room temperature for 60 hours. The solution is concentrtated and the residue is treated with ice and 10% sodium bicarbonate solution and extracted with methylene chloride. The organic solution is dried with sodium sulphate, filtered and concentrated. The residue is purified on a 450 g silica gel column using methylene chloride as the eluting agent and crystallised from ethanol. There is obtained benzyl-rac-{1-[[2-(o-fluorobenzoyl)-4-nitrophenyl]carbamoyl]butyl}carbamate which melts at 148°-150° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04281188
出典データセットuspto-grants-1981_07
ORD IDord-8a2a8b6b0dac4d13ac301f6c849ef9b1
出典メモuspto-grants-1981_07