Pentane → HCID 131720371, compound

HRID 1421339Notes

Reaction equation

HRID 1421339 reaction equation
[CH3:1][C:2]1[C:3]([CH3:20])=[C:4]([CH3:19])[C:5]([Si:8]([NH:11][C:12]2[CH:17]=[CH:16][C:15]([F:18])=[CH:14][CH:13]=2)([CH3:10])[CH3:9])([CH3:7])[CH:6]=1.CCCCC.C([Li:30])CCC>C(OCC)C.CCCCCC>[CH3:1][C:2]1[C:3]([CH3:20])=[C:4]([CH3:19])[C:5]([Si:8]([N-:11][C:12]2[CH:13]=[CH:14][C:15]([F:18])=[CH:16][CH:17]=2)([CH3:10])[CH3:9])([CH3:7])[CH:6]=1.[Li+:30].[Li+:30].[CH3:1][C:2]1[C:3]([CH3:20])=[C:4]([CH3:19])[C:5]([Si:8]([N-:11][C:12]2[CH:13]=[CH:14][C:15]([F:18])=[CH:16][CH:17]=2)([CH3:10])[CH3:9])([CH3:7])[CH:6]=1

Participants

6

Procedure

((Tetramethylcyclopentadienyl)dimethylsilyl)-(4-fluorophenyl)amine in diethyl ether solvent and butyl lithium 2.5 M in hexane solvent were combined in equivalent amounts. A white precipitate formed. Pentane was added to the slurry. The precipitate was filtered, washed with pentane and dried. 1H NMR (THF-d8) δ 7.28 (m, 2.0), 6.77 (m, 2), 3.27 (s, 2.7), 2.05 (s, 5.2), 2.01(s, 5.2), 0.44 (s, 4.6)

Workup

  1. customA white precipitate formed
  2. filtrationThe precipitate was filtered
  3. washwashed with pentane
  4. customdried

Sources & evidence

ORD record
ord-3cb1cafa40994d3fbc4ea75f0c43434f
Source dataset
uspto-grants-2000_06
Patent number
US06075077

Reaction notes

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