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HRID 1866613作成日:2026年10月25日

Hydrogen Peroxide → Benzyl 5-hydroxy-2,2-dimethylpentanoate

https://huagongshe.com/reaction/1866613

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen PeroxideHCID 784—
反応物9-Borabicyclo(3.3.1)nonaneHCID 78966—
反応物Sodium AcetateHCID 517045—
反応物Benzyl 2,2-dimethylpent-4-enoateHCID 66973286—
溶媒TetrahydrofuranHCID 8028—
生成物Benzyl 5-hydroxy-2,2-dimethylpentanoateHCID 66972971—

反応手順

To a solution of benzyl 2,2-dimethylpent-4-enoate (5.74 g, 26.3 mmol, prepared according to Step A) in THF (100 mL) was added a solution of 9-BBN (63.1 mL, 31.6 mmol, 0.5 M in THF) over 20 minutes, while under nitrogen. The reaction was allowed to stir at ambient temperature for 17 hours. An aqueous solution of sodium acetate (7.3 g, 89 mmol, in 18 mL of water) was then added, followed by the slow addition of aqueous hydrogen peroxide (18 mL, 30% by weight solution) with occasional chilling in a 0° C. bath. This mixture was allowed to stir at ambient temperature for 1.5 hours, before being extracted with ethyl acetate. The combined organics were washed with saturated brine. The organics were then dried over sodium sulfate, filtered, and concentrated in vacuo to give a residue that was purified by silica gel chromatography, eluting with a gradient of MeOH:DCM—1:99 to 10:90, to give the title compound. MS: m/z=237 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07629338B2
出典データセットuspto-grants-2009_12
ORD IDord-6a8db5db14804a738b46f0f98418a88e
出典メモuspto-grants-2009_12