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HRID 335538作成日:2026年10月25日

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

https://huagongshe.com/reaction/335538

反応式

関与物質

役割名称HCID仕込み量
反応物1-Bromo-3-chloropropaneHCID 8006—
反応物5-(Tetradecyloxy)-2-furoic acidHCID 115175—
反応物Tetrabutylammonium hydroxide pentahydrateHCID 86669148—
触媒Sodium IodideHCID 5238—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
溶媒Sodium chloride; waterHCID 57417360—
生成物3-Chloropropyl 5-(tetradecyloxy)furan-2-carboxylateHCID 6686984469.1%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08884034B2
出典データセットuspto-grants-2014_11
ORD IDord-f789956f17f64916aecb4bd78346b715
出典メモuspto-grants-2014_11