HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233601Generated: October 30, 2026
Sulfuric Acid → 4-Bromo-6-chloro-2,3-dihydro-2,2-dimethylbenzofuran
https://huagongshe.com/reaction/233601
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 7-Amino-4-bromo-6-chloro-2,3-dihydro-2,2-dimethylbenzofuran | HCID 53705332 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Bromo-6-chloro-2,3-dihydro-2,2-dimethylbenzofuran | HCID 53688294 | 0.2% |
Reaction Steps
A stirred solution of 5.1 grams (0.01 8 mole) of 7-amino-4-bromo-6-chloro-2,3-dihydro-2,2-dimethylbenzofuran and 25 mL of toluene in 100 mL of ethanol is cooled in an ice bath, and 2 mL (0.036 mole) of concentrated sulfuric acid is added slowly. Upon completion of addition, 2.0 grams (0.029 mole) of sodium nitrite is then added. The ice bath is then removed, and the reaction mixture is warmed to 75° C., where it is stirred for 30 minutes. After this time the reaction mixture is warmed to 95° C., where it stirred for one hour. The reaction mixture is then cooled and poured into 200 mL of water. The mixture is extracted with two 150 mL portions of diethyl ether. The combined extracts are dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure to a residue. The residue is subjected to column chromatography on silica gel. Elution is accomplished using petroleum ether. The product-containing fractions are combined and concentrated under reduced pressure, yielding 3.6 grams of 4-bromo-6-chloro-2,3-dihydro-2,2-dimethylbenzofuran. The NMR spectrum is consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05593998 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-2f757d112f3545a9878ffbca29de8f02 |
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| Source note | uspto-grants-1997_01 |
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