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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 57215Erstellt: 24. Oktober 2026

1-Bromo-3-chloropropane → 3-Chloropropyl 5-(tetradecyloxy)furan-2-carboxylate

https://huagongshe.com/de/reaction/57215

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Bromo-3-chloropropaneHCID 8006—
Edukt5-(Tetradecyloxy)-2-furoic acidHCID 115175—
EduktTetrabutylammonium hydroxide pentahydrateHCID 86669148—
KatalysatorSodium IodideHCID 5238—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelSodium chloride; waterHCID 57417360—
Produkt3-Chloropropyl 5-(tetradecyloxy)furan-2-carboxylateHCID 6686984469,1%

Reaktionsschritte

To a vigorously stirred suspension of 5-(tetradecyloxy)furan-2-carboxylic acid (0.650 g, 2.0 mmol) in 10 mL of N,N-dimethylformamide was added 3-chlorobromopropane (0.618 mL, 6.0 mmol), tetrabutylammonium hydroxide pentahydrate (0.734 g, 4.2 mmol) and sodium iodide (˜20 mg). The suspension appeared to go into solution briefly, and then a very finely dispersed white precipitate was observed. The reaction was allowed to stir for 12 hrs. The suspension was then diluted with EtOAc (100 mL), brine (50 mL) and water (50 mL). The phases were separated and the organic phase was washed with water (50 mL) and brine (50 mL). The organic phase was then dried and concentrated to yield 0.554 g of the title compound. This material was used in the subsequent step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434718B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-d415c70e93b2457da7ef6543791e7477
Quellennotizuspto-grants-2016_09