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HRID 539979作成日:2026年10月25日

Toluene → (S)-4-(benzylamino-methyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/539979

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物BenzylamineHCID 7504—
反応物3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, (S)-(-)-HCID 179824—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒1,2-DichloroethaneHCID 11—
溶媒WaterHCID 962—
生成物(S)-4-(benzylamino-methyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl esterHCID 6871432560.8%

反応手順

A mixture of tert-butyl (4S)-4-formyl-2,2-dimethyl-1,3-oxazolidine-3-carboxylate (1.0 g, 4.36 mmol), phenylmethanamine (491 mg, 4.58 mmol) and toluene (8 mL) was heated under reflux with stirring for 2 hours. The mixture was concentrated in vacuo. The residue was dissolved in 1,2-dichloroethane (10 mL), to which sodium bis(acetyloxy)boranuidyl acetate (2.31 g, 10.91 mmol) was added. The mixture was stirred at room temperature for two days, then diluted with water (25 mL), extracted with dichloromethane (25 mL×3). The combined organic layers were washed with brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by flash column chromatography to afford 849 mg of the product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08871756B2
出典データセットuspto-grants-2014_10
ORD IDord-c6e549b9cbae4269af347c35b8df2406
出典メモuspto-grants-2014_10