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HRID 1045335作成日:2026年10月27日

Sodium Hydroxide → HCID 58264321、化合物

https://huagongshe.com/reaction/1045335

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物Glyceryl Allyl EtherHCID 78950—
反応物Linoleyl methanesulfonateHCID 59753235—
触媒Tetrabutylammonium hydrogen sulfateHCID 94433—
溶媒TolueneHCID 1140—
生成物HCID 58264321HCID 58264321—

反応条件

温度2.5 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08569256B2
出典データセットuspto-grants-2013_10
ORD IDord-afd5f79a56104055a1a2250e6860e35d
出典メモuspto-grants-2013_10