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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Bromo-4-chloro-2,3-dihydro-2,2-dimethyl-7-nitrobenzofuran | HCID 22404815 | — |
| Catalyst | Silver tetrafluoroborate | HCID 159722 | — |
| Product | 4-Chloro-2,3-dihydro-2,2-dimethyl-7-nitrobenzofuran-3-one | HCID 22404810 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05521147 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-f911b54315eb4438875afbb8c0854477 |
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| Source note | uspto-grants-1996_05 |
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