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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091163Generated: November 1, 2026

Thionyl Chloride → 5-Chloro-2-(1-chloro-3-methylbutyl)-3-methyl-1-benzofuran

https://huagongshe.com/reaction/2091163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 66777421HCID 66777421—
SolventTolueneHCID 1140—
Product5-Chloro-2-(1-chloro-3-methylbutyl)-3-methyl-1-benzofuranHCID 6677844696%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution (10 mL) of 1-(5-chloro-3-methyl-1-benzofuran-2-yl)-3-methylbutan-1-ol (650 mg) synthesized above in toluene was added thionyl chloride (225 μL), and the mixture was stirred at 50° C. for 2 hr. The reaction mixture was poured into ice-cooled saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure to give the title object compound (668 mg, 96%) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-94c05cc2d0e544d29384b8c5df6a4ddb
Source noteuspto-grants-2013_05