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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 63321Erstellt: 23. Oktober 2026

Potassium Carbonate → Cyclohexylmethyl 5-bromofuran-2-carboxylate

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt5-Bromo-2-furanecarboxylic acidHCID 68511—
EduktCyclohexane, (bromomethyl)-HCID 137636—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
ProduktCyclohexylmethyl 5-bromofuran-2-carboxylateHCID 86694615—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09447078B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-49f17556297445d296f005a98aae47f5
Quellennotizuspto-grants-2016_09