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ChemicalBook CAS DataBase List Ethyl 3-bromo-2-oxobutyrate
57332-84-0

Ethyl 3-bromo-2-oxobutyrate synthesis

3synthesis methods
-

Yield:57332-84-0 97%

Reaction Conditions:

with bromine in dichloromethane at 5 - 20;

Steps:

1.A
Step A: Ethyl 3-bromo-2-oxobutanoate (1-B). To a solution of compound 1-A (4.8 g, 36.9 mmol) in CH2Cl2 (20 mL), cooled to 5° C., was added bromine (1.89 mL, 36.9 mmol), drop-wise. The reaction mixture was allowed to warm to room temperature and stir for 18 h. The reaction mixture was purged with nitrogen, diluted with EtOAc, and the organic phase washed with 10% NaHCO3 (2*), H2O, brine, dried over Na2SO4, filtered and the solvent evaporated under reduced pressure to afford compound 1-B as a yellow oil (7.50 g, 97%). 1H-NMR (CDCl3): δ 5.15-5.20 (q, 1H), 4.32-4.45 (m, 2H), 1.82-1.85 (d, 3H), 1.38-1.41 (t, 3H).

References:

Macielag, Mark J.;Xia, Mingde;McNally, James J.;Matthews, Jay M. US2012/149699, 2012, A1 Location in patent:Page/Page column 14-15

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