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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1045335생성일: 2026년 10월 26일

Sodium Hydroxide → HCID 58264321, 화합물

https://huagongshe.com/reaction/1045335

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Glyceryl Allyl EtherHCID 78950—
반응물Linoleyl methanesulfonateHCID 59753235—
촉매Tetrabutylammonium hydrogen sulfateHCID 94433—
용매TolueneHCID 1140—
생성물HCID 58264321HCID 58264321—

반응 조건

온도2.5 °C

반응 단계

In a 2000 mL round bottom flask equipped with a large magnetic stir bar, 3-allyloxypropane-1,2-diol (5.94 g, 45 mmol), and tetrabutylammonium hydrogen sulfate (6 g, 18 mmol) were added. A solution of linoleyl mesylate (33.8 g, 98 mmol) in toluene (150 mL) was also made and added. The mixture was cooled to 0-5° C. with an ice bath. 50% sodium hydroxide (70 mL) was then slowly added, rinsing in with deionized water (20 mL). The resulting mixture is stirred at room temperature, under nitrogen for 40 hours. Deionized water (200 mL) and isopropyl acetate (200 mL) were added and the mixture stirred vigorously for a further 10-15 min. The mixture was transferred to a 1000-mL separating funnel and allowed to separate. The aqueous phase was removed and the organic phase washed with saturated sodium chloride solution (2×150 mL). The organic phase was dried with magnesium sulfate (40 g), filtered, and concentrated to obtain a neat orange oil. The oil was purified by column chromatography. Final yield: 19.5 g (69%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08569256B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-afd5f79a56104055a1a2250e6860e35d
출처 메모uspto-grants-2013_10