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HRID 65138作成日:2026年10月25日

Hydrochloric Acid → N-Acetyl-L-phenylalanine

https://huagongshe.com/reaction/65138

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Potassium CarbonateHCID 11430—
反応物4-benzylidene-2-methyl-4H-oxazol-5-oneHCID 94946—
反応物HCID 178418361HCID 178418361—
触媒HCID 178418390HCID 178418390—
溶媒WaterHCID 962—
生成物N-Acetyl-L-phenylalanineHCID 74839157.7%

反応手順

In 100-ml tightly-sealed glass vessel were charged 9.36 g of 2-methyl-4-benzylidene-5-oxazolone and 40 ml of water. 4.15 g of potasium carbonate was then added thereto and the resulting mixture was stirred at 40°-45° C. for two hours. Concentrated hydrochloric acid was added to the resulting solution to adjust its pH at 6.8 and 0.2 g of 5%-palladium-carbon was added thereto. The gas phase in the vessel was purged with nitrogen and then with hydrogen, and thereafter the reaction mixture in the vessel was subjected to catalytic reduction at 40°-45° C. under atmospheric pressure. The reaction time during which hydrogen absorption was completed was 100 minutes. It was observed that one mole of hydrogen was absorbed to one mole of 2-methyl-4-benzylidene-5-oxazolone during this period. After the gas phase in the vessel was purged with nitrogen upon completion of the reaction, the catalyst was filtered and washed with a small amount of water. The filtrate and the washings were combined, to which concentrated hydrochloric acid was added at a temperature lower than 30° C. to adjust pH of the resulting mixture at 1. The mixture was cooled to 0°-5° C. The crystal was filtered, washed with a cold water and dried to obtain 9.81 g of N-acetylphenylalanine having a melting point 150°-151° C. as a white crystal. Its yield was 94.7%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04612388
出典データセットuspto-grants-1986_09
ORD IDord-8dc93d17569e4c1ca7a56b900e05279f
出典メモuspto-grants-1986_09