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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 62712Erstellt: 24. Oktober 2026

Bromocyclopentane → Methyl 3,5-dichloro-4-(cyclopentyloxy)benzoate

https://huagongshe.com/de/reaction/62712

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromocyclopentaneHCID 8728—
EduktPotassium CarbonateHCID 11430—
EduktMethyl 3,5-dichloro-4-hydroxybenzoateHCID 76856—
LösungsmittelDimethylformamideHCID 6228—
ProduktMethyl 3,5-dichloro-4-(cyclopentyloxy)benzoateHCID 6704155984,2%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

Methyl 3,5-dichloro-4-hydroxybenzoate (1) (1.00 g, 4.52 mmol) was dissolved in DMF (8 mL) and treated with bromocyclopentane (534 μL, 4.98 mmol), followed by potassium carbonate (937 mg, 6.79 mmol). The mixture was stirred at 80° C. for 3 h and then partitioned between EtOAc (100 mL) and H2O (100 mL). The aqueous phase was extracted with EtOAc (50 mL) and the combined organic phases washed successively with water (5×50 mL) and brine (50 mL), then dried over MgSO4 and filtered. The solvent was removed in vacuo to afford methyl 3,5-dichloro-4-(cyclopentyloxy)benzoate (2) (1.10 g, 84%): 1H NMR (400 MHz, CDCl3) δ: 7.97 (2H, s), 5.04 (1H, m), 3.90 (3H, s), 2.04-1.91 (4H, m), 1.82-1.75 (2H, m), 1.69-1.60 (2H, m).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09447028B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-1ce85cf82a9243398065a499278f6629
Quellennotizuspto-grants-2016_09