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ChemicalBook CAS DataBase List BOC-L-4-Nitrophe
33305-77-0

BOC-L-4-Nitrophe synthesis

5synthesis methods
Di-tert-butyl dicarbonate

24424-99-5

4-Nitro-3-phenyl-L-alanine

949-99-5

BOC-L-4-Nitrophe

33305-77-0

To a stirred solution of 4.0 g of (S)-2-amino-3-(4-nitrophenyl)propanoic acid (0.019 mol) in 30 cm3 tert-butanol and 0.8 g of NaOH (0.0209 mol, dissolved in 5 cm3 of water) was added slowly and dropwise at 0 °C 5 cm3 of di-tert-butyl dicarbonate (0.0228 mol, dissolved in 5 cm3 of tert-butanol). The reaction mixture was stirred for 10 h at room temperature. After completion of the reaction (confirmed by thin layer chromatography), the solvent was removed by evaporation and the residue was poured into water and extracted with ethyl acetate (2 x 50 cm3). The organic phases were combined, washed sequentially with 50 cm3 10% citric acid solution and 50 cm3 saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give (S)-2-((tert-butoxycarbonyl)amino)-3-(4-nitrophenyl)propionic acid as a white solid. Yield: 5.0 g (86% yield); Melting point: 105-106°C (literature value 105-107°C).

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Yield:33305-77-0 88%

Reaction Conditions:

in tetrahydrofuran;sodium hydroxide

Steps:

48.A (S)-N-boc-4-nitrophenylalanine
Example 48A (S)-N-boc-4-nitrophenylalanine To a solution of (S)-4-nitrophenylalanine (2.00 g, 9.51 mmol) in aqueous 2M NaOH (10 mL) and THF (5 mL), was added di-tertbutyldicarbonate (2.00 g, 9.17 mmol) in THF (5 mL). The reaction was stirred at ambient temperature for 1 hour, diluted with H2O (25 mL) and 1M HCl (25 mL), extracted with ether (3*25 mL). The combined ether layers were extracted with brine (1*25 mL), dried (MgSO4), filtered, and concentrated under reduced pressure to provide the titled compound (2.51 g, 88%).

References:

Liu, Gang;Szczepankiewicz, Bruce G.;Pei, Zhonghua;Xin, Zhili;Oost, Thorsten K.;Janowick, David A. US2002/35137, 2002, A1

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