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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 612980생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/612980

반응식

참여 물질

역할이름HCID투입량
반응물2-Chlorobenzoyl chlorideHCID 69110—
반응물3-Methyl-1-(2,4,6-trichlorophenyl)-1H-pyrazol-5-amineHCID 2060032—
반응물Aluminum(III) ChlorideHCID 6451240—
용매1,1,2,2-TetrachloroethaneHCID 6591—
생성물5-(2-Chlorobenzamido)-4-(2-chlorobenzoyl)-3-methyl-1-(2,4,6-trichlorophenyl)pyrazoleHCID 1842779251.2%

반응 단계

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 C24H14O2N3Cl5 : C, 52.06: H, 2.55; N, 7.59. Found: C, 52.11; H, 2.57; N, 7.27.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06005109
출처 데이터셋uspto-grants-1999_12
ORD IDord-98d86e7905c64621b4eadc2f11106529
출처 메모uspto-grants-1999_12