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1,3-Cyclopentadiene, 1-propyl → HCID 178440519, compound

HRID 735297
Notes
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Reaction equation

HRID 735297 reaction equation
[Cl-].[Cl-].[Cl-].[Cl-].[Cl-].[Ta+5].C([Mg]Br)(C)C.C(C1([Li])C=CC=C1)CC.C(C1CC=CC=1)CC.C([Li])CCC.Cl[Ta:35](Cl)([C:44]1([CH2:49][CH2:50][CH3:51])[CH:48]=[CH:47][CH:46]=[CH:45]1)[C:36]1([CH2:41][CH2:42][CH3:43])[CH:40]=[CH:39][CH:38]=[CH:37]1.[H-].COCCO[Al+]OCCOC.[Na+].[H-]>CCOCC.C1COCC1.O.C1(C)C=CC=CC=1>[CH2:49]([C:44]1([TaH3:35][C:36]2([CH2:41][CH2:42][CH3:43])[CH:40]=[CH:39][CH:38]=[CH:37]2)[CH:48]=[CH:47][CH:46]=[CH:45]1)[CH2:50][CH3:51]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

12

Reactant 7

HCID 5281711,3-Cyclopentadiene, 1-propylHCID 10269745Einecs 254-460-4HCID 21584525Sodium bis(2-methoxyethoxy)aluminiumhydrideHCID 178418339ButyllithiumHCID 178418365HCID 178418365, compoundHCID 178440518HCID 178440518, compound
HCID 178506698
HCID 178506698, compound

Product 1

HCID 178440519HCID 178440519, compoundYield 12.8%

Reagents, catalysts & solvents 4

HCID 962WaterSolventHCID 1140TolueneSolvent2×HCID 3283Diethyl EtherSolventHCID 8028TetrahydrofuranSolvent

Conditions

Temperature
-70 °C

Procedure

80.0 g (223 mmol) of tantalum pentachloride was suspended in 1,340 ml of ether, and 324 ml (220 mmol) of isopropyl magnesium bromide (0.68M THF solution) was added thereto. A solution of 50.2 g (440 mmol) of propylcyclopentadienyl lithium prepared from propylcylopentadiene and butyl lithium in THF (380 ml) was added, followed by refluxing for 1 hour. The solvent was distilled away, and the residue was dried at 80° C. in vacuo for 8 hours to obtain a brownish-red solid containing dichlorobis(propylcyclopentadienyl)tantalum (Ta (PrCp)2Cl2). 2,100 ml of toluene was added to this brownish-red solid, and the resulting mixture was ice-cooled. 198 ml (660 mmol) of a toluene solution (65 wt %) of sodium bis(2-methoxyethoxy)aluminum hydride was added dropwise to the mixture, and temperature was returned to room temperature, followed by stirring for 19.5 hours. 106 ml of water was added to the mixture, followed by stirring until foaming does not occur. Insoluble contents were filtered out, and the solvent was distilled away from the filtrate. 2,000 ml of hexane was added to the residue, the insoluble contents were filtered out, and the filtrate was concentrated to about 800 ml. When the concentrated liquid was cooled to −70° C., a white solid was formed. A supernatant was removed, and the solid was washed with 40 ml of cold pentane two times to obtain 11.2 g (yield: 12.8%) of a white solid.

Workup

  1. additionwas added
  2. temperatureby refluxing for 1 hour
  3. distillationThe solvent was distilled away
  4. customthe residue was dried at 80° C. in vacuo for 8 hours
  5. customto obtain a brownish-red solid
  6. temperaturecooled
  7. customwas returned to room temperature
  8. stirringby stirring until foaming
  9. filtrationInsoluble contents were filtered out
  10. distillationthe solvent was distilled away from the filtrate
  11. addition2,000 ml of hexane was added to the residue
  12. filtrationthe insoluble contents were filtered out
  13. concentrationthe filtrate was concentrated to about 800 ml
  14. customa white solid was formed
  15. customA supernatant was removed
  16. washthe solid was washed with 40 ml of cold pentane two times

Sources & evidence

ORD record
ord-2f8e4317321b4a978412bc900f9ff358
Source dataset
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07592471B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes