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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554229Generated: October 28, 2026

Cyclohexyl bromide → HCID 66925034, compound

https://huagongshe.com/reaction/554229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexyl bromideHCID 7960—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantEthyl 1H-pyrrole-3-carboxylateHCID 13070719—
SolventCarbon DisulfideHCID 6348—
ProductHCID 66925034HCID 6692503416%

Reaction Conditions

Temperature50 °C

Reaction Steps

Under an argon atmosphere, to a solution of ethyl 1H-pyrrole-3-carboxylate (2.09 g) and aluminum(III) chloride (4.0 g) in carbon disulfide (30 mL) was added bromocyclohexane (1.84 mL) under ice-cooling with stirring, and the mixture was stirred at room temperature for 30 min. The mixture was heated to 50° C., and stirred for 2 hr. The reaction product was cooled to room temperature, poured into ice water, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=19:1→8:2), and recrystallized from hexane to give the title compound as a colorless solid (yield 530 mg, 16%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048909B2
Source datasetuspto-grants-2011_11
ORD IDord-62cee19ab8e14936ba829df650d901c8
Source noteuspto-grants-2011_11