Pentane → HCID 131720369, compound

HRID 2119986Notes

Reaction equation

HRID 2119986 reaction equation
[CH3:1][C:2]1[C:3]([CH3:21])=[C:4]([CH3:20])[C:5]([Si:8]([NH:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[O:18][CH3:19])([CH3:10])[CH3:9])([CH3:7])[CH:6]=1.C([Li:26])CCC.CCCCC>C(OCC)C.CCCCCC>[CH3:1][C:2]1[C:3]([CH3:21])=[C:4]([CH3:20])[C:5]([Si:8]([N-:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[O:18][CH3:19])([CH3:10])[CH3:9])([CH3:7])[CH:6]=1.[Li+:26].[Li+:26].[CH3:1][C:2]1[C:3]([CH3:21])=[C:4]([CH3:20])[C:5]([Si:8]([N-:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[O:18][CH3:19])([CH3:10])[CH3:9])([CH3:7])[CH:6]=1

Participants

6

Procedure

To 1.4 g (4.6 mmol) ((tetramethylcyclopentadienyl)dimethylsilyl) (2-methoxyphenyl)amine in diethyl ether was added dropwise 3.9 mL of 2.5 M butyl lithium (9.8 mmol) in hexane solvent. A white precipitate formed. Pentane was added to the mixture. The slurry was filtered and the solids washed with pentane.

Workup

  1. customA white precipitate formed
  2. filtrationThe slurry was filtered
  3. washthe solids washed with pentane

Sources & evidence

ORD record
ord-eef03e2e18b04e6c819ade2f679863a2
Source dataset
uspto-grants-2004_02
Patent number
US06686488B2

Reaction notes

Loading…