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HRID 67265作成日:2026年10月25日

Phenol → Phenyl 1-(4-Chlorophenyl)-1,4-dihydro-4-oxo-6-methylpyridazine-3-carboxylate

https://huagongshe.com/reaction/67265

反応式

関与物質

役割名称HCID仕込み量
反応物PhenolHCID 996—
反応物TriethylamineHCID 8471—
反応物Phenyl chloroformateHCID 15891—
反応物FenridazonHCID 197225—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒HexaneHCID 8058—
生成物Phenyl 1-(4-Chlorophenyl)-1,4-dihydro-4-oxo-6-methylpyridazine-3-carboxylateHCID 919200619.1%

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 125 mol of toluene there is added dropwise 3.13 g (0.02 mol) of phenyl chloroformate. The suspension formed is stirred at room temperature for 15 minutes and to it there is added 1.88 g (0.02 mol) of phenol in 25 ml of toluene. The mixture is stirred at room temperature for 18 hrs. and to it there is added 100 ml of water. The suspension is stirred at room temperature for 2 hrs. and is poured into 800 ml of hexane. The suspension formed is stirred at room temperature for 3 hrs. and is vacuum filtered. The filter cake is slurried in 25 ml of toluene and is filtered. The filtrate is added to 150 ml of hexane and the suspension formed is stirred at room temperature for 2 hrs. The suspension is vacuum filtered and the filter cake air dried to afford 1.3 g (19% yield) of product, mp 140°-146° 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-e9b5717f5d59430f8f2ec1312dd35dfb
出典メモuspto-grants-1982_08