Diisopropylamine → HCID 66747345, compound

HRID 591204Notes

Reaction equation

HRID 591204 reaction equation
C(NC(C)C)(C)C.C([Li])CCC.[CH3:13][O:14][C:15]1[CH:16]=[C:17]([CH:21]([CH2:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)[C:22]#[N:23])[CH:18]=[CH:19][CH:20]=1.Br[CH2:32][C:33]([O:35][CH3:36])=[O:34]>O1CCCC1.Cl>[CH3:36][O:35][C:33](=[O:34])[CH2:32][C:21]([CH2:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)([C:22]#[N:23])[C:17]1[CH:18]=[CH:19][CH:20]=[C:15]([O:14][CH3:13])[CH:16]=1

Participants

7

Procedure

To a solution of diisopropylamine (0.7 ml, 5.1 mmol) in 20 ml dry tetrahydrofuran at −78° C. was added n-butyl lithium (1.6 M in hexan, 3.2 ml, 5.1 mmol) and stirred for 1 h. A solution of 2-(3-methoxy-phenyl)-3-phenyl-propionitrile (1.0 g, 4.2 mmol) in 5 ml dry tetrahydrofuran was added to the mixture, stirred for 30 min, followed by addition of methyl 2-bromoacetate (0.6 ml, 6.3 mmol). The mixture was stirred over night at room temperature, diluted with 50 ml 1M HCl and the resulting mixture extracted with dichloromethane. The organic layer was washed with water and brine, dried over sodium bicarbonate, filtered and the solvent evaporated to obtain a yellow oil (1.3 g). Purification on 12 g SiO2 using dichloromethane afforded a clear colourless oil.

Workup

  1. stirringstirred for 30 min
  2. stirringThe mixture was stirred over night at room temperature
  3. extractionthe resulting mixture extracted with dichloromethane
  4. washThe organic layer was washed with water and brine
  5. dry with materialdried over sodium bicarbonate
  6. filtrationfiltered
  7. customthe solvent evaporated

Sources & evidence

ORD record
ord-bc35fd66c24842f7b05ed2297cad59f9
Source dataset
uspto-grants-2016_01
Patent number
US09238619B2

Reaction notes

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