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HRID 727387作成日:2026年10月26日

2-Chlorobenzoyl chloride → 5-(2-Chlorobenzamido)-4-(2-chlorobenzoyl)-3-methyl-1-(2,4,6-trichlorophenyl)pyrazole

https://huagongshe.com/reaction/727387

反応式

関与物質

役割名称HCID仕込み量
反応物2-Chlorobenzoyl chlorideHCID 69110—
反応物3-Methyl-1-(2,4,6-trichlorophenyl)-1H-pyrazol-5-amineHCID 2060032—
反応物Aluminum(III) ChlorideHCID 6451240—
溶媒1,1,2,2-TetrachloroethaneHCID 6591—
生成物5-(2-Chlorobenzamido)-4-(2-chlorobenzoyl)-3-methyl-1-(2,4,6-trichlorophenyl)pyrazoleHCID 1842779251.2%

反応手順

A suspension of 2.34 g (17.50 mmol) of aluminum trichloride in 20 mL of 1,1,2,2-tetrachloroethane was treated with 2.02 mL (2.78 g, 15.9 mmol) of 2-chlorobenzoyl chloride and the resulting solution was stirred for 20 minutes at room temperature. Then 2.00 g (7.23 mmol) of the product of Step A was added and the reaction mixture was refluxed for 16 hours. The cooled reaction mixture was poured over ice and the insolubles were filtered off and washed with ethyl acetate. The organic layer was separated and the aqueous was washed twice with ethyl acetate. The combined organic layers were dried over magnesium sulfate and evaporated. The residues were chromatographed on silica gel, eluting with 4:1 hexane ethyl acetate to give 2.05 g (51%) of the title product, an amorphous foam. Anal. Calcd. for C24N14O2N3Cl5 : C, 52.06; H, 2.55; N, 7.59. Found: C, 52.11; H, 2.57; N, 7.27.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05712303
出典データセットuspto-grants-1998_01
ORD IDord-00aff6261ec046d3a6549c48b117080f
出典メモuspto-grants-1998_01