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HRID 67263作成日:2026年10月24日

Cyclohexanol → Cyclohexyl 1-(4-chlorophenyl)-1,4-dihydro-4-oxo-6-methylpyridazine-3-carboxylate

https://huagongshe.com/ja/reaction/67263

反応式

関与物質

役割名称HCID仕込み量
反応物CyclohexanolHCID 7966—
反応物TriethylamineHCID 8471—
反応物Carbonochloridic acid, cyclohexyl esterHCID 83262—
反応物FenridazonHCID 197225—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒HexaneHCID 8058—
生成物Cyclohexyl 1-(4-chlorophenyl)-1,4-dihydro-4-oxo-6-methylpyridazine-3-carboxylateHCID 1308412265%

反応手順

To an ice cooled suspension of 5.29 g (0.02 mol) 1-(4-chlorophenyl)-1,4-dihydro-4-oxo-6-methyl pyridazine-3-carboxylic Acid (see Example 12) and 2.02 g (0.02 mol) of triethylamine in 75 ml of toluene there is added 3.25 g (0.02 mol) of cyclohexyl chloroformate. The suspension formed is stirred at room temperature for 15 minutes and to it there is added 3.2 g (0.022 mol) of cyclohexanol in 50 ml of toluene. The mixture is stirred at room temperature for 38 hrs. and to it there is added 100 ml of water. The mixture is stirred at room temperature for 1 hr. and the toluene layer is isolated and poured into 600 ml of hexane. The suspension formed is stirred at room temperature for 1/2 hr. and is vacuum filtered. The filter cake is air dried to afford 4.5 g (65% yield) of product, mp 160°-162° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04345934
出典データセットuspto-grants-1982_08
ORD IDord-1ff062a96b93482eaad2b50dc2687f39
出典メモuspto-grants-1982_08