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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 335538생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/335538

반응식

참여 물질

역할이름HCID투입량
반응물1-Bromo-3-chloropropaneHCID 8006—
반응물5-(Tetradecyloxy)-2-furoic acidHCID 115175—
반응물Tetrabutylammonium hydroxide pentahydrateHCID 86669148—
촉매Sodium IodideHCID 5238—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
용매Sodium chloride; waterHCID 57417360—
생성물3-Chloropropyl 5-(tetradecyloxy)furan-2-carboxylateHCID 6686984469.1%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08884034B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-f789956f17f64916aecb4bd78346b715
출처 메모uspto-grants-2014_11