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HRID 1981290作成日:2026年10月25日

Imidazole → Climbazole

https://huagongshe.com/reaction/1981290

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物WaterHCID 962—
反応物1-Bromo-1-(4-chlorophenoxy)-3,3-dimethylbutan-2-oneHCID 13269143—
反応物Imidazoyl ketoneHCID 21924262—
溶媒AcetonitrileHCID 6342—
生成物ClimbazoleHCID 37907—

反応手順

The antigingivitis agent utilized in present invention is 1-imidazoyl-(p-chlorophenoxy)3-3-dimethyl 2-butanone having the structural formula: ##STR2## which is prepared by reacting 1-bromo-1-(4-chlorophenoxy)-3,3-dimethyl-2-butanone with imidazole dissolved in acetonitrile as disclosed in U.S. Pat. Nos. 3,812,142 and 3,903,287, which is made a part of this specification. This imidazoyl ketone is a water insoluble crystalline powder having a melting point of 94.5°-97.8° C. which may be obtained from the Bayer Company as Climbazole. Due to the water insolubility of this imidazole compound, it must first be solubilized in a nonionic compound prior to the addition of ionic materials in an aqueous medium.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04514382
出典データセットuspto-grants-1985_04
ORD IDord-0c06c30f47d243f7943f6a72356ccafd
出典メモuspto-grants-1985_04