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HRID 1972323作成日:2026年10月25日

Benzyl Bromide → (S)-benzyl 2-(dibenzylamino)pentanoate

https://huagongshe.com/reaction/1972323

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Potassium CarbonateHCID 11430—
反応物Sodium HydroxideHCID 14798—
反応物L-NorvalineHCID 65098—
溶媒WaterHCID 962—
生成物(S)-benzyl 2-(dibenzylamino)pentanoateHCID 44223288132.9%

反応条件

温度0 °C

反応手順

Sodium hydroxide (0.513 Kg; 12.82 moles) and potassium carbonate (1.77 Kg, 12.82 moles) were dissolved in water (7.5 L) and cooled to 0° C. The resulting solution was treated with (S)-2-aminopentanoic acid (L-norvaline, 0.75 Kg; 6.41 moles) slowly at between 0-5° C. The stirred suspension was heated at 90° C. and benzyl bromide (4.385 Kg, 25.64 moles) was added dropwise. Heating was continued for a further 12 hours at 90° C. The reaction mixture was then cooled to ambient temperature, and extracted with ethyl acetate (2×6 liters). The layers were separated and the aqueous phase extracted twice with ethyl acetate. The combined organic extracts were dried over sodium sulfate, and the solvent removed under reduced pressure to obtain 3.3 Kg of crude (S)-benzyl 2-(dibenzylamino)pentanoate, a compound of formula (3), as a brown oil. This material was used in the next reaction without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08431733B2
出典データセットuspto-grants-2013_04
ORD IDord-f7b38c2c6f8f4157bf7f2030d294d5a7
出典メモuspto-grants-2013_04