돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4521생성일: 2026년 10월 24일

Dimethyl Sulfoxide → 7-Benzo[1,3]dioxol-5-yl-7-pyridin-3-yl-hept-6-enoic acid

https://huagongshe.com/ko/reaction/4521

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물Sodium hydrideHCID 24758—
반응물(5-Carboxypentyl)triphenylphosphanium bromideHCID 2779280—
반응물(2H-1,3-Benzodioxol-5-yl)(pyridin-3-yl)methanoneHCID 13285824—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물7-Benzo[1,3]dioxol-5-yl-7-pyridin-3-yl-hept-6-enoic acidHCID 1328583124.6%

반응 조건

온도85 °C

반응 단계

Sodium hydride (1 g, 60% in oil) was added to dimethyl sulfoxide (25 ml) under nitrogen and the mixture was heated at 85° C. with stirring for an hour. The reaction mixture was cooled to room temperature and 5-carboxypentyltriphenylphosphonium bromide (5.2 g, 11 mmoles) was added gradually. The mixture was stirred for 10 minutes and a solution of 3-(3,4-methylenedioxybenzoyl)pyridine (2.5 g, 0.11 mole) in tetrahydrofuran (10 ml) was added dropwise thereto. After completion of addition, the mixture was further stirred at room temperature for 30 minutes. After completion of the reaction, water (100 ml was added and the neutral substance was extracted twice with toluene (50 ml). The aqueous layer was adjusted to pH 5.5 with 2N hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with water, dried (magnesium sulfate) and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography using ethyl acetate as the eluent. The eluate was concentrated and the residue was crystallized from ethyl acetate-isopropyl ether to give (Z)-7-(3,4-methylenedioxyphenyl)-7-(3-pyridyl)-6-heptenoic acid (0.4 g, 24.6%). Mp 90°-91° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04727078
출처 데이터셋uspto-grants-1988_02
ORD IDord-a74b6d8de3c74927ba4f80b2e8d86f3c
출처 메모uspto-grants-1988_02