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HRID 1726678作成日:2026年10月25日

Sodium Iodide → 1-Benzyl 4-(tert-Butyl) N-Benzyl-N-(2-(chloromethyl)allyl)-L-aspartate

https://huagongshe.com/reaction/1726678

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物Potassium CarbonateHCID 11430—
反応物3-Chloro-2-chloromethyl-1-propeneHCID 15859—
反応物1-Benzyl 4-(tert-butyl) benzyl-L-aspartateHCID 16069553—
溶媒AcetonitrileHCID 6342—
生成物1-Benzyl 4-(tert-Butyl) N-Benzyl-N-(2-(chloromethyl)allyl)-L-aspartateHCID 1606955458.3%

反応条件

温度81 °C

反応手順

Part 2: A mixture of (2S)-benzylamino-succinic acid 1-benzyl ester 4-tert-butyl ester (12.1 g, 32.6 mmol), K2CO3 (14 g, 3 equiv.), NaI (3.0 g, 20 mmol) and 3-chloro-2-chloromethyl-1-propene (5.1 g, 40.8 mmol) in MeCN (150 mL) was stirred at 81° C. for 16 h. After cooling, the reaction mixture was filtered and the filtrate was concentrated under reduced pressure. Purification by Combiflash (hexane and ethyl acetate: gradient 0 to 8% during 12 min) afforded (2S)-[benzyl-(2-chloromethyl-allyl)-amino]-succinic acid 1-benzyl ester 4-tert-butyl ester (8.7 g, 58%). MS (ESI): 458 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07491724B2
出典データセットuspto-grants-2009_02
ORD IDord-dd8e7c51cf4841bf8701b067addce352
出典メモuspto-grants-2009_02