Isobutyric Acid → HCID 19047496, compound
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
Reactant 6
Product 1
Reagents, catalysts & solvents 1
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
- temperatureTo the mixture cooled to -78° C.
- customThe mixture was quenched with 1N HCl
- temperaturewarmed to room temperature
- extractionextracted with ether (3×50ml)
- dry with materialThe organic layer was dried over magnesium sulfate
- concentrationconcentrated in vacuo
- 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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