戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 488154作成日:2026年10月23日

Sodium hydride → Dimethyl [1-acetyl-4,8,12-trimethyltrideca-3,7,11-trienyl]phosphonate

https://huagongshe.com/ja/reaction/488154

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物Dimethyl (2-oxopropyl)phosphonateHCID 77872—
反応物Farnesyl bromideHCID 550199—
溶媒TetrahydrofuranHCID 8028—
生成物Dimethyl [1-acetyl-4,8,12-trimethyltrideca-3,7,11-trienyl]phosphonateHCID 53770837—

反応条件

温度20 °C

反応手順

Dimethyl 2-oxopropylphosphonate (560 μL, 4.0 mmol) was added dropwise to a stirred suspension of sodium hydride (50% oil suspension, prewashed with hexane) (210 mg, 4.8 mmol) in anhydrous THF (15 mL) at 20° C. under an Argon atmosphere. The resulting slurry was stirred at 20° C. for 2 hours to allow for complete formation of the sodio derivative and then treated dropwise with farnesyl bromide (1.14 mL, 4.2 mmol). The cloudy yellow mixture was stirred at 20° C. for 2 hours and then quenched with saturated NH4Cl solution. The resulting mixture was washed with water, dried, filtered and evaporated to give the crude product which was purified by flash chromatography on a silica gel column. Elution of the column with hexane:ethyl acetate:methanol (40:10:1, v:v:v) gave the title compound as gum.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05298655
出典データセットuspto-grants-1994_03
ORD IDord-37315ade40574a3dab8693161682355a
出典メモuspto-grants-1994_03