戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1769263作成日:2026年10月26日

Dicyclohexylcarbodiimide → 2-Allyloxy-1-methylethyl 5-chloroquinolin-8-oxyacetate

https://huagongshe.com/reaction/1769263

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物3-Pyridinamine, N,N-dimethyl-HCID 123378—
反応物2-Propanol, 1-(2-propenyloxy)-HCID 542178—
反応物CloquintocetHCID 15257197—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物2-Allyloxy-1-methylethyl 5-chloroquinolin-8-oxyacetateHCID 1548412972.4%

反応条件

温度0 °C

反応手順

5.0 g (0.021 mol) of 5-chloroquinolin-8-oxyacetic acid and 2.44 g (0.021 mol) of 2-allyloxy-1-methylethanol are suspended in a mixture of 40 ml of methylene chloride and 40 ml of dimethylformamide and the suspension is cooled to 0° C. 4.78 g (0.023 mol) of dicyclohexylcarbodiimide, dissolved in 10 ml of methylene chloride, are added dropwise at this temperature, and 200 mg of 3-(N,N-dimethylamino)-pyridine are then added. The mixture is stirred at room temperature for 15 hours and the precipitate which has separated out is filtered off with suction and rinsed with 50 ml of methylene chloride. The filtrate is washed with 100 ml of 0.5 N HCl, with 100 ml of potassium bicarbonate solution and with 3 portions of in each case 50 ml of water. The organic phase is dried over magnesium sulfate and the solvent is stripped off in vacuo. The residue is recrystallized from n-heptane. 5.1 g (72.4% of theory) of 2-allyloxy-1-methylethyl 5-chloroquinolin-8-oxyacetate of melting point 59° C. are obtained in this manner.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05380852
出典データセットuspto-grants-1995_01
ORD IDord-df1b135afad3466692a98882f3761cf4
出典メモuspto-grants-1995_01