Hydrogen Bromide → L-Phenylalanine-amide hydrobromide

反応式

[CH:1]1[CH:6]=[CH:5][C:4]([CH2:7][C@H:8]([NH:12]C(OCC2C=CC=CC=2)=O)[C:9]([NH2:11])=[O:10])=[CH:3][CH:2]=1.[BrH:23]>C(O)(=O)C.CCOCC>[BrH:23].[NH2:12][C@H:8]([C:9]([NH2:11])=[O:10])[CH2:7][C:4]1[CH:5]=[CH:6][CH:1]=[CH:2][CH:3]=1

参加物

実験手順

6.55 g (22 mmoles) of Z--Phe--NH2, prepared as described in Example 1, Step 1, are dissolved in 13 ml of acetic acid, and 30 ml of 5 n hydrogen bromide in acetic acid are added to the solution. After 5 minutes of stirring a thick precipitate separates. The suspension is allowed to stand for one hour, thereafter it is diluted with dry ether and filtered. The crude product is dissolved in 240 ml of ethanol, the solution is decolorized, and the product is precipitated with 740 ml of ether. 4.90 g (91 %) of H--Phe--NH2.HBr are obtained; the white, crystalline substance is chromatographically uniform. (Two spots appear on the thin layer chromatogram: one of them belongs to the product and the other to hydrogen bromide). M.P.: 249-250° C., Rf8 : 0.50; Rf8,HBr: 0.35.