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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2380332생성일: 2026년 10월 26일

Hydrochloric Acid → Sodium 2-{3-[(4,6-diphenyl-2-pyridyl)oxy]propyloxy}acetate

https://huagongshe.com/reaction/2380332

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium HydroxideHCID 14798—
반응물3-[(4,6-Diphenyl-2-pyridyl)oxy]-1-propanolHCID 18987283—
반응물Potassium tert-butoxideHCID 23665647—
반응물Potassium 2-bromoacetateHCID 23681702—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매tert-ButanolHCID 6386—
생성물Sodium 2-{3-[(4,6-diphenyl-2-pyridyl)oxy]propyloxy}acetateHCID 23712831—

반응 조건

온도100 °C

반응 단계

To potassium tert-butylate (5.52 g) in tert-butanol (60 cc) heated to 100° C. is added, in the form of a homogeneous solid, a mixture of 3-[(4,6-di-phenyl-2-pyridyl)oxy]-1-propanol (5 g) and potassium 2-bromoacetate (4.35 g). The addition is carded out in 1 hour. The reaction mixture is then heated for 48 hours at 100° C. and then poured in iced water (100 g). The pH of the aqueous phase is brought to 5 by addition of 1N hydrochloric acid. The mixture is then extracted with dichloromethane (3×50 cc) after saturating the aqueous phase with sodium chloride. The combined organic phases are dried over sodium sulphate and concentrated to dryness at 40° C. under reduced pressure. The oily residue obtained is purified by chromatography under pressure on silica gel (30-60 mm; eluent: n-hexane-diethyl ether 65-35 and then 40-60 and then diethyl ether-methanol; 9-1). The white solid obtained, taken up in acetone (5 cc), is treated with sodium hydroxide pellets (0.19 g) and distilled water (1. cc). The mixture is stirred for 60 hours at room temperature. The precipitate obtained is filtered, washed with ethyl ether and dried at 40° C. under reduced pressure. (white solid; m.p.=285°-288° C.)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05366982
출처 데이터셋uspto-grants-1994_11
ORD IDord-505724630e3147829fcc8b2e25cd99a2
출처 메모uspto-grants-1994_11