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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52655Generated: October 25, 2026

Sulfuric Acid → 4-Bromo-2,2-dimethyl-2,3-dihydrobenzofuran

https://huagongshe.com/reaction/52655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantTolueneHCID 1140—
ReactantSodium NitriteHCID 23668193—
Reactant7-Amino-4-bromo-2,3-dihydro-2,2-dimethylbenzofuranHCID 53722008—
SolventEthanolHCID 702—
Product4-Bromo-2,2-dimethyl-2,3-dihydrobenzofuranHCID 5398912731.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

A stirred solution of 12.3 grams (0.051 mole) of 7-amino-4-bromo-2,3-dihydro-2,2-dimethylbenzofuran and 30 mL of toluene in 200 mL of ethanol was cooled in an ice-bath, and 5.6 mL (0.102 mole) of concentrated sulfuric acid was added slowly, followed by 5.6 grams (0.082 mole) of sodium nitrite. Upon completion of addition, the ice-bath was removed, and the reaction mixture was warmed to 50° C. The reaction mixture temperature was then brought to about 75° C., where it was stirred for 30 minutes. After this time the reaction mixture was heated at reflux for one hour and then was poured into 200 mL of water. The mixture was extracted with two 150 mL portions of diethyl ether. The combined extracts were dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to a residual oil. The oil was subjected to column chromatography on silica gel. Elution was accomplished using petroleum ether. The product-containing fractions were combined and concentrated under reduced pressure, yielding 3.6 grams of 4-bromo-2,3-dihydro-2,2-dimethylbenzofuran. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616718
Source datasetuspto-grants-1997_04
ORD IDord-a1b606ee6ad447b19aaba25f27f2e464
Source noteuspto-grants-1997_04