Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091429Generated: November 1, 2026

Nitromethane → Cyclohexyl(6-methoxy-2-methyl-1-benzofuran-3-yl)methanone

https://huagongshe.com/reaction/2091429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitromethaneHCID 6375—
ReactantCyclohexanecarbonyl chlorideHCID 75938—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant6-Methoxy-2-methylbenzofuranHCID 13013073—
SolventWaterHCID 962—
ProductCyclohexyl(6-methoxy-2-methyl-1-benzofuran-3-yl)methanoneHCID 6677815847%

Reaction Steps

To a mixture of 6-methoxy-2-methyl-1-benzofuran (1.50 g), cyclohexanecarbonyl chloride (1.36 mL) and nitromethane (15 mL) was added aluminum chloride (1.85 g) at 0° C., and the mixture was stirred for 1 hr. Water 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. The residue was purified by silica gel column chromatography (0-10% ethyl acetate/hexane) to give the title object compound (1.18 g, 47%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-2e1d509d621f4d1d9635951cfb3a5140
Source noteuspto-grants-2013_05