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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440657Generated: October 29, 2026

Dimethyl Sulfoxide → 4-Chloro-2,3-dihydro-2,2-dimethyl-7-nitrobenzofuran-3-one

https://huagongshe.com/reaction/440657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
Reactant3-Bromo-4-chloro-2,3-dihydro-2,2-dimethyl-7-nitrobenzofuranHCID 22404815—
CatalystSilver tetrafluoroborateHCID 159722—
Product4-Chloro-2,3-dihydro-2,2-dimethyl-7-nitrobenzofuran-3-oneHCID 22404810—

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 15.0 g (0.0489 mole) of 3-bromo-4-chloro-2,3-dihydro-2,2-dimethyl-7-nitrobenzofuran in 100 mL of dimethyl sulfoxide was added slowly to a mixture of 9.73 g (0.050 mole) of silver tetrafluoroborate in 100 mL of dimethyl sulfoxide. Upon completion of addition, 5.0 g (0.050 mole) of triethylamine was added to the reaction mixture, and stirring was continued for approximately 16 hours at ambient temperature. At the conclusion of this period the reaction mixture was heated at 60° C. for one hour and then cooled to ambient temperature. The mixture was filtered, and the filtrate was poured into 200 mL of water. This mixture was extracted with diethyl ether. The extract was dried over anhydrous magnesium sulfate, filtered, and the solvent was evaporated from the filtrate under reduced pressure, leaving a residue. This residue was passed through a column of silica gel, yielding 5.35 g of 4-chloro-2,3-dihydro-2,2-dimethyl-7-nitrobenzofuran-3-one as a solid residue, m.p. 167°-168° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521147
Source datasetuspto-grants-1996_05
ORD IDord-f911b54315eb4438875afbb8c0854477
Source noteuspto-grants-1996_05