Water → HCID 131727126, compound

HRID 2116834Notes

Reaction equation

HRID 2116834 reaction equation
[CH3:1][C:2]1[CH:3]([C:10]2[CH:17]=[CH:16][CH:15]=[CH:14][C:11]=2[C:12]#[N:13])[C:4]([CH3:9])=[C:5]([CH3:8])[C:6]=1[CH3:7].[CH3:18][C:19]1[CH:24]=[C:23]([CH3:25])[CH:22]=[C:21]([CH3:26])[C:20]=1[Li].C1(C)C=CC=CC=1.O>O1CCCC1>[CH3:1][C:2]1[CH:3]([C:10]2[CH:17]=[CH:16][CH:15]=[CH:14][C:11]=2[C:12]([C:20]2[C:21]([CH3:26])=[CH:22][C:23]([CH3:25])=[CH:24][C:19]=2[CH3:18])=[NH:13])[C:4]([CH3:9])=[C:5]([CH3:8])[C:6]=1[CH3:7]

Participants

6

Reactant 4

HCID 962WaterHCID 1140TolueneHCID 131727127HCID 131727127, compoundHCID 178506704HCID 178506704, compound

Product 1

HCID 131727126HCID 131727126, compoundYield 108.1%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Procedure

To a solution of 2-(2,3,4,5-tetramethylcyclopentadienyl)benzonitrile (6.3 mmol) in tetrahydrofuran (25.5 mL) was added dropwise a solution of 2,4,6-trimethylphenyllithium (12.5 mmol) in tetrahydrofuran (55.6 mL) at −78° C. under a nitrogen atmosphere. The temperature of the mixture was raised to room temperature and the mixture was stirred for 5 hrs. To the reaction mixture solution were added toluene and water to separate an organic layer and an aqueous layer. The organic layer was dried and the solvent was distilled off to give 2-(2,3,4,5-tetramethylcyclopentadienyl)-α-(2,4,6-trimethylphenyl) -benzenemethanimine (2.34 g) as a brown oily substance.

Workup

  1. customto separate an organic layer
  2. customThe organic layer was dried
  3. distillationthe solvent was distilled off

Sources & evidence

ORD record
ord-7f3ed3984b9645c4940d471b87f0ec7a
Source dataset
uspto-grants-2008_10
Patent number
US07439379B2

Reaction notes

Loading…