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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954745Generated: October 26, 2026

Diazoacetophenone → Ethyl 4-(4-chloro-2-nitrobenzoyl)-3-benzoyl-1H-pyrazole-5-carboxylate

https://huagongshe.com/reaction/1954745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazoacetophenoneHCID 18667—
ReactantEthyl 4-(4-chloro-2-nitrophenyl)-4-oxo-2-butynoateHCID 18358889—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-(4-chloro-2-nitrobenzoyl)-3-benzoyl-1H-pyrazole-5-carboxylateHCID 1835888474.3%

Reaction Steps

A solution of ethyl 4-(4-chloro-2-nitrophenyl)-4-oxo-2-butynoate (prepared as described in Example 48(a)) (1.2 g, 4.11 mmol) and diazoacetophenone (1.2 g 8.22 mmol, prepared as described in Org. Syn. Coll. Vol. VI. pp. 386-388) in tetrahydrofiuran (THF) (21.6 mL) was stirred at room temperature for 16 hours. The reaction was concentrated by rotary evaporation and purified by flash chromatography eluting with hexanes:ethyl acetate (90:10, 80:20, 70:30) to give the title compound (1.3 g, 74.3%); Rf 0.38 (1:1 ethyl acetate:hexanes).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124281
Source datasetuspto-grants-2000_09
ORD IDord-490c052ab35b44f6bc8df66c6d9ae89a
Source noteuspto-grants-2000_09