Ethyl Acetate → HCID 59492364, compound

HRID 1951542Notes

Reaction equation

HRID 1951542 reaction equation
[CH2:1]([C:3]1[S:7][C:6]([CH3:8])=[N:5][CH:4]=1)[CH3:2].C([Li])CCC.[C:14](OCC)(=[O:16])[CH3:15]>C1COCC1>[CH2:1]([C:3]1[S:7][C:6]([CH2:8][C:14]([CH3:15])=[O:16])=[N:5][CH:4]=1)[CH3:2]

Participants

5

Conditions

Temperature
-78 °C

Procedure

600 mg (4.72 mmol) of 5-ethyl-2-methyl-1,3-thiazole [M. Poite et al., Bull. Chem. Soc. Fr., 2078-2085 (1962)] are dissolved in 20 ml of abs. THF and, at −78° C., 2.08 ml (5.18 mmol) of n-butyllithium (2.5 M solution in hexane) are added dropwise. After stirring at −78° C. for two hours, 706 mg (8.02 mmol) of ethyl acetate are added as a solution in 10 ml of abs. THF. The mixture is stirred at −78° C. for 1 h and then warmed to room temperature. It is then hydrolyzed with sodium bicarbonate solution, and the mixture is extracted three times with diethyl ether. The combined organic phases are dried with magnesium sulfate, and the solvent is removed in a rotary evaporator. The crude product is purified by MPLC (Biotage 40M cartridge, eluent: isohexane/ethyl acetate 80:20). 50 mg (6% of theory) of the title compound are obtained.

Workup

  1. stirringThe mixture is stirred at −78° C. for 1 h
  2. temperaturewarmed to room temperature
  3. extractionhydrolyzed with sodium bicarbonate solution, and the mixture is extracted three times with diethyl ether
  4. dry with materialThe combined organic phases are dried with magnesium sulfate
  5. customthe solvent is removed in a rotary evaporator
  6. customThe crude product is purified by MPLC (Biotage 40M cartridge, eluent: isohexane/ethyl acetate 80:20)

Sources & evidence

ORD record
ord-5eba03934ca2497493d9d2aa6be88a52
Source dataset
uspto-grants-2013_03
Patent number
US08404723B2

Reaction notes

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