Fluorene → HCID 18469391, compound

HRID 1899383Notes

Reaction equation

HRID 1899383 reaction equation
[CH:1]1[C:13]2[CH2:12][C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[CH:4]=[CH:3][CH:2]=1.C([Li])CCC.[Br:19][CH:20](Br)[CH3:21].[NH4+].[Cl-]>O1CCCC1.CCCCC>[Br:19][CH2:20][CH2:21][C:1]1[C:13]2[CH2:12][C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[CH:4]=[CH:3][CH:2]=1

Participants

7

Procedure

In this reaction, 8.3 g (0.05 m) of fluorene was dissolved in 150 ml of tetrahydrofuran. The 31.8 ml (0.05 m) of butyl lithium (1.6 molar in hexane) was added dropwise to this solution. After one hour, this solution was added gradually to a stirred solution of 9 ml (0.1 m) of dibromoethane in 300 ml of pentane within 2 hours. Then the reaction mixture was treated with 50 ml of an aqueous NH4Cl solution, and then washed with 50 ml of water. The organic phase was dried over Na2SO4. Then the solvent was removed in vacuo. The yellow residue was dissolved in pentane. The pentane solution was filtered over silica. The solution was concentrated to about 20% of the original volume and then the product was crystallized at -30° C. A yield of 10.88 g of 1-bromo-2-(fluorenyl)ethane was obtained. The product was characterized through

Workup

  1. washwashed with 50 ml of water
  2. dry with materialThe organic phase was dried over Na2SO4
  3. customThen the solvent was removed in vacuo
  4. dissolutionThe yellow residue was dissolved in pentane
  5. filtrationThe pentane solution was filtered over silica
  6. concentrationThe solution was concentrated to about 20% of the original volume
  7. customthe product was crystallized at -30° C

Sources & evidence

ORD record
ord-f97fa02a8dea463983e4fdd9fdd1798f
Source dataset
uspto-grants-1996_11
Patent number
US05571880

Reaction notes

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