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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073899Generated: November 1, 2026

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

https://huagongshe.com/reaction/1073899

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Iodobenzoyl chlorideHCID 69112—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant3,4-dihydro-2,2-dimethyl-4-(2-pyridyl)-2H-1-benzopyranHCID 19895611—
SolventDiethyl EtherHCID 3283—
SolventNitromethaneHCID 6375—
Product3,4-dihydro-2,2-dimethyl-6-(2-iodobenzoyl)-4-(2-pyridyl)-2H-1-benzopyranHCID 1989568746.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

250 mg of 3,4-dihydro-2,2-dimethyl-4-(2-pyridyl)-2H-1-benzopyran were dissolved in 10 ml of nitromethane and cooled in an ice-bath under a nitrogen atmosphere. 280 mg of finely powdered aluminum chloride were added followed, after 5 minutes, by 700 mg of 2-iodobenzoyl chloride. After stirring at 0° C. for 30 minutes and at room temperature for 1 hour the mixture was diluted with diethyl ether and washed with sodium hydroxide solution. The organic phase was dried over sodium sulphate and evaporated. The residue was chromatographed on silica gel using ethyl acetate/petroleum ether (1:2) for the elution to give 230 mg of 3,4-dihydro-2,2-dimethyl-6-(2-iodobenzoyl)-4-(2-pyridyl)-2H-1-benzopyran.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04971982
Source datasetuspto-grants-1990_11
ORD IDord-bbff5863f11a46fbac417c5d9f4087ae
Source noteuspto-grants-1990_11