戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 126879作成日:2026年10月26日

Imidazole → HCID 20286585、化合物

https://huagongshe.com/reaction/126879

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物1,5-Naphthalenedisulfonic acidHCID 6666—
反応物1-Bromo-4-chloro-1-(4-chlorophenoxy)-3,3-dimethyl-butan-2-oneHCID 20286562—
溶媒AcetoneHCID 180—
溶媒AcetonitrileHCID 6342—
生成物HCID 20286585HCID 2028658584.7%

反応手順

17 g (0.05 mol) of crude 1-bromo-1-(4-chlorophenoxy)-3,3-dimethyl-4-chloro-butan-2-one were dissolved in 100 ml of absolute acetonitrile. 12 g (0.175 mol) of imidazole were added to this solution and the mixture was heated under reflux for 40 hours. Thereafter, it was concentrated by distilling off the solvent in vacuo and the residue was taken up in 300 ml of methylene chloride. The methylene chloride mixture was washed three times with 100 ml of water each time, dried over sodium sulphate and concentrated again in vacuo. The residue was taken up in 100 ml of acetone, and a solution of 9 g (0.038 mol) of 1,5-naphthalenedisulphonic acid in 50 ml of acetone was added. After 2 hours, the precipitate which had formed was filtered off and dried. 19.8 g (80.7% of theory) of 1-(4-chlorophenoxy)-1-(imidazol-1-yl)-3,3-dimethyl-4-chloro-butan-2-one naphthalene-1,5-disulphonate of melting point 266°- 267° C. were obtained. ##STR14##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04254132
出典データセットuspto-grants-1981_03
ORD IDord-e16aee086878472a9e58aad7c5ba34c4
出典メモuspto-grants-1981_03