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Ethyl bromoacetate → Ethyl 2-(tetramethylcyclopentadienyl)acetate

HRID 849683
Notes
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Reaction equation

HRID 849683 reaction equation
Br[CH2:2][C:3]([O:5][CH2:6][CH3:7])=[O:4].[CH3:8][C:9]1[CH-:13][C:12]([CH3:14])=[C:11]([CH3:15])[C:10]=1[CH3:16].[Na+]>C1COCC1>[CH3:8][C:9]1[CH:13]([CH2:2][C:3]([O:5][CH2:6][CH3:7])=[O:4])[C:12]([CH3:14])=[C:11]([CH3:15])[C:10]=1[CH3:16]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 7748Ethyl bromoacetateHCID 15823254Tetramethylcyclopentadienylsodium

Product 1

HCID 85614880Ethyl 2-(tetramethylcyclopentadienyl)acetate

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Procedure

A solution of 3.822 g (22.89 mmol) ethyl bromoacetate in 25 mL THF was cooled to -78° C. and 3.000 g (20.80 g) sodium tetramethylcyclopentadienide in 50 mL THF was slowly added to it. The resulting slurry was allowed to warm to room temperature and was stirred overnight. The solvent was removed, the residue was extracted with pentane and filtered. The pentane was removed to give a mixture of isomers. Yield was 3.733 g (86.3%). Mass spectra m/e 208 (41 percent).

Workup

  1. customThe solvent was removed
  2. extractionthe residue was extracted with pentane
  3. filtrationfiltered
  4. customThe pentane was removed
  5. customto give
  6. additiona mixture of isomers

Sources & evidence

ORD record
ord-09c41894aba443eeb1f3f3ae50c825e6
Source dataset
uspto-grants-2000_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06013819

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes