Isobutyric Acid → HCID 19047496, compound

HRID 742507Notes

Reaction equation

HRID 742507 reaction equation
[CH:1]([N-]C(C)C)(C)C.[Li+].C(NC(C)C)(C)C.[Li]CCCC.[C:21]([OH:26])(=[O:25])[CH:22]([CH3:24])[CH3:23].CN(P(N(C)C)(N(C)C)=O)C.Br[CH2:39][C:40]([O:42][CH2:43][CH2:44][CH2:45][CH2:46][CH2:47][CH2:48][CH2:49][CH3:50])=[O:41]>C1COCC1>[CH2:43]([O:42][C:40]([CH:39]([CH3:1])[C:22]([CH3:24])([CH3:23])[C:21]([OH:26])=[O:25])=[O:41])[CH2:44][CH2:45][CH2:46][CH2:47][CH2:48][CH2:49][CH3:50]

Participants

8

Conditions

Temperature
45 °C

Procedure

To a mixture of lithium diisopropylamide (prepared from 4.8 g, (47.8 mmol) of diisopropylamine and 19.1 ml, (2.5M, 47.8 mmol) of n-BuLi) in 50 ml of THF was added isobutyric acid (2.2 ml, 23.9 mmol) at 0° C. and the mixture was allowed to warm to 45° C. with stirring. To the mixture cooled to -78° C., was added 4.3 g (23.9 mmol) of HMPA followed by a solution of 1-octyl bromoacetate (6 g, 23.9 mmol) in 50 ml of THF under argon at -78° C. The mixture was quenched with 1N HCl, warmed to room temperature, and extracted with ether (3×50ml). The organic layer was dried over magnesium sulfate, concentrated in vacuo, and purified by flash chromatography (10% methanol/ethyl acetate) to afford 0.8 g of 3-(1-octyloxycarbonyl)-2,2-dimethylbutyric acid.

Workup

  1. temperatureTo the mixture cooled to -78° C.
  2. customThe mixture was quenched with 1N HCl
  3. temperaturewarmed to room temperature
  4. extractionextracted with ether (3×50ml)
  5. dry with materialThe organic layer was dried over magnesium sulfate
  6. concentrationconcentrated in vacuo
  7. custompurified by flash chromatography (10% methanol/ethyl acetate)

Sources & evidence

ORD record
ord-490495e422054a60a036740c798b7da7
Source dataset
uspto-grants-1996_09
Patent number
US05554620

Reaction notes

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