Bromine → Ethyl 4-bromo-2-methyl-3-oxopentanoate

HRID 1501783Notes

Reaction equation

HRID 1501783 reaction equation
[CH3:1][CH:2]([C:8](=[O:11])[CH2:9][CH3:10])[C:3]([O:5][CH2:6][CH3:7])=[O:4].[Br:12]Br>C(Cl)(Cl)Cl>[Br:12][CH:9]([CH3:10])[C:8](=[O:11])[CH:2]([CH3:1])[C:3]([O:5][CH2:6][CH3:7])=[O:4]

Participants

4

Procedure

To a solution of ethyl 2-methyl-3-oxopentanoate (5.0 g, 34.7 mmol) in chloroform at 0° C. was added bromine (1.79 mL, 34.7 mmol) in chloroform (10 mL) drop-wise. The resulting solution was stirred at rt for 16 h. The solution was washed with water, dried over sodium sulfate, and concentrated to give the title compound. 1HNMR (500 MHz, CDCl3), δ4.781-4.740 (dd, J=6.6 Hz, 1H), 4.140-4.098(dd, J=7.0 Hz, 1H), 3.770 (s, 3H), 1.797-1.783(d, J=6.6 Hz, 3H), 1.455-1.442 (d, J=7.0 Hz, 3H).

Workup

  1. washThe solution was washed with water
  2. dry with materialdried over sodium sulfate
  3. concentrationconcentrated

Sources & evidence

ORD record
ord-86510c3380014661b9b6ba04a78c6014
Source dataset
uspto-grants-2015_12
Patent number
US09206198B2

Reaction notes

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