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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 63321Generated: October 24, 2026

Potassium Carbonate → Cyclohexylmethyl 5-bromofuran-2-carboxylate

https://huagongshe.com/en/reaction/63321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-2-furanecarboxylic acidHCID 68511—
ReactantCyclohexane, (bromomethyl)-HCID 137636—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductCyclohexylmethyl 5-bromofuran-2-carboxylateHCID 86694615—

Reaction Steps

A mixture of 5-bromofuran-2-carboxylic acid (2.64 g, 13.8 mmol), (cyclohexylmethyl)bromide (2.62 g, 14.8 mmol), K2CO3 (2.30 g, 16.64 mmol) in anhydrous NMP was stirred under Ar at +70° C. for 8 hrs after which additional (cyclohexylmethyl)bromide (1.55 g, 8.75 mmol) was added. Stirring continued overnight then the reaction mixture was concentrated under reduced pressure. The residue was partitioned between aqueous NaHCO3 (10%) and hexanes, and then aqueous layer was extracted with hexanes. Combined organic layers were washed with brine, dried over anhydrous MgSO4 and concentrated under reduced pressure to give cyclohexylmethyl 5-bromofuran-2-carboxylate as a light yellow oil. Yield (2.22 g, 56%); 1H NMR (400 MHz, CDCl3) δ 7.10 (d, J=3.9 Hz, 1H), 6.44 (d, J=3.4 Hz, 1H), 4.10 (d, J=6.4 Hz, 2H), 1.64-1.84 (m, 6H), 1.12-1.34 (m, 3H), 0.95-1.09 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447078B2
Source datasetuspto-grants-2016_09
ORD IDord-49f17556297445d296f005a98aae47f5
Source noteuspto-grants-2016_09