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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091017Generated: October 26, 2026

Hydrochloric Acid → Methyl 3-ethyl-1-benzofuran-2-carboxylate

https://huagongshe.com/reaction/2091017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl bromoacetateHCID 60984—
Reactant2'-HydroxypropiophenoneHCID 69133—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
SolventAcetoneHCID 180—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-ethyl-1-benzofuran-2-carboxylateHCID 6677818252%

Reaction Steps

To a mixture of 1-(2-hydroxyphenyl)propan-1-one (10.0 g), methyl bromoacetate (5.11 mL) and acetone (100 mL) was added potassium carbonate (18.4 g), and the mixture was stirred overnight at room temperature. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:4, volume ratio) to give a colorless oil. To a solution (150 mL) of the obtained oil in N,N-dimethylformamide was added 1,8-diazabicyclo[5.4.0]undec-7-ene (8.12 mL), and the mixture was stirred at 120° C. for 2 hr. 1N Hydrochloric acid was added to quench the reaction, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. Ethyl acetate was added to the residue, the insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:9, volume ratio) to give the title object compound (7.14 g, 52%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-d46a4e17ca2148adbe03cef3788ca2d0
Source noteuspto-grants-2013_05