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HRID 233604作成日:2026年10月25日

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

https://huagongshe.com/reaction/233604

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物TolueneHCID 1140—
反応物Sodium NitriteHCID 23668193—
反応物7-Amino-4-bromo-2,3-dihydro-2,2-dimethylbenzofuranHCID 53722008—
溶媒EthanolHCID 702—
生成物4-Bromo-2,2-dimethyl-2,3-dihydrobenzofuranHCID 5398912731.1%

反応条件

温度50 °C

反応手順

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 is cooled in an ice-bath, and 5.6 mL (0.102 mole) of concentrated sulfuric acid is added slowly, followed by 5.6 grams (0.082 mole) of sodium nitrite. Upon completion of addition, the ice-bath is removed, and the reaction mixture is warmed to 50° C. The reaction mixture temperature is then brought to about 75° C., where it is stirred for 30 minutes. After this time the reaction mixture is heated at reflux for one hour and then is 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 residual oil. The oil 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-2,3-dihydro-2,2-dimethylbenzofuran. The NMR spectrum is consistent with the proposed structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05593998
出典データセットuspto-grants-1997_01
ORD IDord-1e00cde85a8b4418948718126feeb20a
出典メモuspto-grants-1997_01