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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57215Generated: October 25, 2026

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

https://huagongshe.com/reaction/57215

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
Reactant5-(Tetradecyloxy)-2-furoic acidHCID 115175—
ReactantTetrabutylammonium hydroxide pentahydrateHCID 86669148—
CatalystSodium IodideHCID 5238—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
Product3-Chloropropyl 5-(tetradecyloxy)furan-2-carboxylateHCID 6686984469.1%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434718B2
Source datasetuspto-grants-2016_09
ORD IDord-d415c70e93b2457da7ef6543791e7477
Source noteuspto-grants-2016_09