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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantTolueneHCID 1140—
ReactantSodium NitriteHCID 23668193—
Reactant7-Amino-4-bromo-6-chloro-2,3-dihydro-2,2-dimethylbenzofuranHCID 53705332—
SolventEthanolHCID 702—
Product4-Bromo-6-chloro-2,3-dihydro-2,2-dimethylbenzofuranHCID 536882940.2%

Reaction Conditions

Temperature75 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05593998
Source datasetuspto-grants-1997_01
ORD IDord-2f757d112f3545a9878ffbca29de8f02
Source noteuspto-grants-1997_01