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HRID 127241作成日:2026年10月26日

Imidazole → 4-Chloro-1-[4-(4-chlorophenyl)-phenoxy]-3,3-dimethyl-1(imidazol-1-yl)-butan-2-one naphthalene-1,5-disulphonate

https://huagongshe.com/reaction/127241

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-(4-chlorophenyl)-phenoxy]-3,3-dimethyl-butan-2-oneHCID 20286578—
溶媒AcetoneHCID 180—
溶媒AcetonitrileHCID 6342—
生成物4-Chloro-1-[4-(4-chlorophenyl)-phenoxy]-3,3-dimethyl-1(imidazol-1-yl)-butan-2-one naphthalene-1,5-disulphonateHCID 2028659474.6%

反応手順

20.8 g (0.05 mol) of crude 1-bromo-4-chloro-1-[4-(4-chlorophenyl)-phenoxy]-3,3-dimethyl-butan-2-one were dissolved in 120 ml of absolute acetonitrile. 12 g (0.175 mol) of imidazole were added and the mixture was heated for 40 hours under reflux. It was then concentrated by distilling off the solvent in vacuo and the residue was taken up in 300 ml of methylene chloride. The solution was washed three times with 100 ml of water at a time and was dried over sodium sulphate and again concentrated 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 formed was filtered off and dried. 19.6 g (72% of theory) of 4-chloro-1-[4-(4-chlorophenyl)-phenoxy]-3,3-dimethyl-1(imidazol-1-yl)-butan-2-one naphthalene-1,5-disulphonate of melting point 246° C. were obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04255434
出典データセットuspto-grants-1981_03
ORD IDord-2bd6031018d24b218f83506fc1e70011
出典メモuspto-grants-1981_03