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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52649Generated: October 30, 2026

Sulfuric Acid → 4-Bromo-6-chloro-2,3-dihydro-2,2-dimethylbenzofuran

https://huagongshe.com/reaction/52649

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 5368829476.5%

Reaction Conditions

Temperature75 °C

Reaction Steps

A stirred solution of 5.1 grams (0.018 mole) of 7-amino-4-bromo-6-chloro-2,3-dihydro-2,2-dimethylbenzofuran and 25 mL of toluene in 100 mL of ethanol was cooled in an ice bath, and 2 mL (0.036 mole) of concentrated sulfuric acid was added slowly. Upon completion of addition, 2.0 grams (0.029 mole) of sodium nitrite was then added. The ice bath was then removed, and the reaction mixture was warmed to 75° C., where it stirred for 30 minutes. After this time the reaction mixture was warmed to 95° C., where it stirred for one hour. The reaction mixture was then cooled and 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 residue. The residue 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-6-chloro-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-5eddf7418b044d549a8eb181a1c08fba
Source noteuspto-grants-1997_04