HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440653Generated: October 29, 2026
4-Chloro-2,3-dihydro-2,2-dimethyl-7-nitrobenzofuran → 7-Amino-4-chloro-2,3-dihydro-2,2-dimethylbenzofuran
https://huagongshe.com/reaction/440653
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chloro-2,3-dihydro-2,2-dimethyl-7-nitrobenzofuran | HCID 22404776 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-Amino-4-chloro-2,3-dihydro-2,2-dimethylbenzofuran | HCID 22404773 | 68.9% |
Reaction Steps
A solution of 4.0 g (0.018 mole) of 4-chloro-2,3-dihydro-2,2-dimethyl-7-nitrobenzofuran in approximately 60 mL of glacial acetic acid was heated to 50° C. To this solution were added 10 mL of water, and, while maintaining the temperature at 50° C., 4.0 g (0.072 mole) of powdered iron. Upon completion of addition, the reaction mixture was allowed to cool to room temperature at which it stirred for an hour. Then the reaction mixture was diluted with 100 mL of water and filtered. The filtrate was extracted with diethyl ether, and the combined extracts were dried over anhydrous magnesium sulfate and filtered. The solvent was evaporated from this filtrate under reduced pressure, leaving 2.45 g of 7-amino-4-chloro-2,3-dihydro-2,2-dimethylbenzofuran as a residue.
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-8324d1a6e5fe4377b4603c87d7f3917a |
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| Source note | uspto-grants-1996_05 |
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