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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Chlorobenzoyl chloride | HCID 69110 | — |
| 反応物 | 3-Methyl-1-(2,4,6-trichlorophenyl)-1H-pyrazol-5-amine | HCID 2060032 | — |
| 反応物 | Aluminum(III) Chloride | HCID 6451240 | — |
| 溶媒 | 1,1,2,2-Tetrachloroethane | HCID 6591 | — |
| 生成物 | 5-(2-Chlorobenzamido)-4-(2-chlorobenzoyl)-3-methyl-1-(2,4,6-trichlorophenyl)pyrazole | HCID 18427792 | 51.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05712303 |
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| 出典データセット | uspto-grants-1998_01 |
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| ORD ID | ord-00aff6261ec046d3a6549c48b117080f |
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| 出典メモ | uspto-grants-1998_01 |
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