Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091132Generated: November 1, 2026

Pyridine → 2-(1-Chloro-3-methylbutyl)-5-methoxy-3-methyl-1-benzofuran

https://huagongshe.com/reaction/2091132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(5-Methoxy-3-methyl-1-benzofuran-2-yl)-3-methylbutan-1-olHCID 66777775—
SolventTolueneHCID 1140—
Product2-(1-Chloro-3-methylbutyl)-5-methoxy-3-methyl-1-benzofuranHCID 6677821894%

Reaction Steps

To a solution (10 mL) of 1-(5-methoxy-3-methyl-1-benzofuran-2-yl)-3-methylbutan-1-ol (761 mg) synthesized above in toluene were added pyridine (297 μL) and thionyl chloride (268 μL), and the mixture was stirred at room temperature for 3 hr. Saturated aqueous sodium hydrogen carbonate solution was added to quench the reaction, and the reaction 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 (769 mg, 94%) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-f894c2d06abe48b0944b97c5cb90df45
Source noteuspto-grants-2013_05