Diisopropylamine → 1,4-Bis(2-carbomethoxy-2-methylpropyl)benzene

HRID 2419854Notes

Reaction equation

HRID 2419854 reaction equation
C(N[CH:5]([CH3:7])[CH3:6])(C)C.C([Li])CCC.[C:13]([O:18][CH3:19])(=[O:17])[CH:14]([CH3:16])[CH3:15].Br[CH2:21][C:22]1[CH:27]=[CH:26][C:25]([CH2:28]Br)=[CH:24][CH:23]=1>CCCCCC.O1CCCC1>[C:13]([C:5]([CH3:6])([CH3:7])[CH2:21][C:22]1[CH:27]=[CH:26][C:25]([CH2:28][C:14]([CH3:16])([C:13]([O:18][CH3:19])=[O:17])[CH3:15])=[CH:24][CH:23]=1)([O:18][CH3:19])=[O:17]

Participants

7

Reactant 4

HCID 7912DiisopropylamineHCID 11039Methyl isobutyrateHCID 693351,4-Bis(bromomethyl)benzeneHCID 178418339Butyllithium

Product 1

HCID 213125761,4-Bis(2-carbomethoxy-2-methylpropyl)benzeneYield 86.1%

Reagents, catalysts & solvents 2

HCID 8028TetrahydrofuranSolventHCID 8058HexaneSolvent

Conditions

Temperature
-78 °C

Procedure

To 1 liter of dry tetrahydrofuran was added 52 g of diisopropylamine. The mixture was cooled to -78° C and 325 ml of 1.6 M n-butyllithium in hexane was added. After 1 hour of stirring 50 g of methyl isobutyrate was added dropwise followed by stirring for another 30 minutes. Then 63 g of α,α'-dibromo-p-xylene was slowly added. The reaction mixture was stirred overnight and brought to room temperature. The mixture was filtered and solvent was removed from the filtrate by evaporation. The residue was recrystallized from methanol to obtain 63 g of 1,4-bis(2-carbomethoxy-2-methylpropyl)benzene, m.p. 74°-76° C.

Workup

  1. additionwas added dropwise
  2. stirringThe reaction mixture was stirred overnight
  3. custombrought to room temperature
  4. filtrationThe mixture was filtered
  5. customsolvent was removed from the filtrate by evaporation
  6. customThe residue was recrystallized from methanol

Sources & evidence

ORD record
ord-e62049c803f147a19a6052eda8b3aa5e
Source dataset
uspto-grants-1978_08
Patent number
US04107444

Reaction notes

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