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ChemicalBook CAS DataBase List Benzenebutanoicacid,b-aMino-2,4,5-trifluoro-,Methylester,(bR)-

Benzenebutanoicacid,b-aMino-2,4,5-trifluoro-,Methylester,(bR)- synthesis

11synthesis methods
(R)-Methyl 3-aMino-4-(2,4,5-trifluorophenyl) butanoate .(R)-2-hydroxy-2-phenylacetate

1253055-94-5
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Benzenebutanoicacid,b-aMino-2,4,5-trifluoro-,Methylester,(bR)-

881995-69-3
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Yield: 95%

Reaction Conditions:

with sodium carbonate in water; pH=8 - 9

Steps:


Methyl(3R)-3-amino-4-(2,4,5-trifluorophenyl)butanoate (31) The methyl(3R)-3-amino-4-(2,4,5-trifluorophenyl)butanoate (R)-(-)-mandelate (30) (113.0 gm) was taken in water (10.0 vol, 1.13 Ltr) and the suspension was stirred for 10-15 minutes. The suspension was further basified by using a 10% Na2CO3 solution (1.0 vol, 113.0 ml) until the pH of the reaction mixture reached 8-9. The product was extracted in ethyl acetate (2*10.0 vol, 2*1.13 Ltr). The combined ethyl acetate layers were further washed with water (2*10.0 vol, 2*1.13 Ltr). The product was isolated as a pale yellow oil by complete distillation of the ethyl acetate under reduced pressure at 45-50° C. Molar Yield: 90-95% (65.0 gm) Chemical Purity: 99-99.5% (as measured by HPLC) Enantiomeric Purity: 99.25-99.75% (as measured by chiral HPLC)

References:

Mylan India Private Limited US2012/108598, 2012, A1 Location in patent:Page/Page column 10

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