HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 63321Erstellt: 23. Oktober 2026
Potassium Carbonate → Cyclohexylmethyl 5-bromofuran-2-carboxylate
https://huagongshe.com/de/reaction/63321
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 5-Bromo-2-furanecarboxylic acid | HCID 68511 | — |
| Edukt | Cyclohexane, (bromomethyl)- | HCID 137636 | — |
| Lösungsmittel | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Produkt | Cyclohexylmethyl 5-bromofuran-2-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09447078B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-49f17556297445d296f005a98aae47f5 |
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| Quellennotiz | uspto-grants-2016_09 |
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