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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892536Generated: October 30, 2026

4-Nitrobenzoyl chloride → 3,4-dihydro-2,2-dimethyl-6-(4-nitrobenzoyl)-4-(2-pyridyl)-2H-1-benzopyran

https://huagongshe.com/reaction/892536

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzoyl chlorideHCID 8502—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant3,4-dihydro-2,2-dimethyl-4-(2-pyridyl)-2H-1-benzopyranHCID 19895611—
SolventNitromethaneHCID 6375—
Product3,4-dihydro-2,2-dimethyl-6-(4-nitrobenzoyl)-4-(2-pyridyl)-2H-1-benzopyranHCID 1989564046.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

200 mg of 3,4-dihydro-2,2-dimethyl-4-(2-pyridyl)-2H-1-benzopyran were dissolved in 10 ml of nitromethane and the solution was cooled to 0° C. under a nitrogen atmosphere. 240 mg of finely powdered aluminum chloride were added and, after stirring at 0° C. for 5 minutes, 388 mg of 4-nitrobenzoyl chloride were added. After 16 hours at room temperature 120 mg of aluminum chloride were added and the mixture was stirred at 100° C. for 45 minutes. After dilution with diethyl ether and washing with sodium hydroxide solution the organic phase was dried over sodium sulphate and evaporated. The residue crystallized and was triturated with diethyl ether to give 150 mg of 3,4-dihydro-2,2-dimethyl-6-(4-nitrobenzoyl)-4-(2 -pyridyl)-2H-1benzopyran.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05118694
Source datasetuspto-grants-1992_06
ORD IDord-1b64f74aa52f47039e9bcbb18cffd2df
Source noteuspto-grants-1992_06