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Sodium, 2,4-cyclopentadien-1-yl- → 2-methoxyethylcyclopentadiene

HRID 2395215
Notes
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Reaction equation

HRID 2395215 reaction equation
[CH3:1][O:2][CH2:3][CH2:4]OS(C1C=CC(C)=CC=1)(=O)=O.[CH-:16]1[CH:20]=[CH:19][CH:18]=[CH:17]1.[Na+]>C1COCC1>[CH3:1][O:2][CH2:3][CH2:4][C:16]1[CH2:20][CH:19]=[CH:18][CH:17]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 78681Sodium, 2,4-cyclopentadien-1-yl-HCID 86977Ethanol, 2-methoxy-, 1-(4-methylbenzenesulfonate)

Product 1

HCID 108968552-methoxyethylcyclopentadieneYield 44%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Conditions

Temperature
0 °C

Procedure

To a solution of 19.7 g(85.7 mmol) 2-methoxyethyltosylate as prepared in step (a) in 200 ml THF cooled to 0° C. was added 55 ml of 2.0M (110 mmol) sodium cyclopentadienylide in THF. The reaction mixture was allowed to warm to room temperature and was stirred for 16 h. 100 ml concentrated aqueous saline solution was added and the product extracted with diethyl ether (3×75 ml). The combined organic fractions were dried over sodium sulphate for 16 hrs, filtered and the solvents removed under reduced pressure using a rotary evaporator to yield a brown oil. The crude product was distilled under reduced pressure (b.p. 40-°44° C. at 2-3 mm Hg) to give 4.5 g of a colourless oil (37.7 mmol, 44.0%).

Workup

  1. temperatureto warm to room temperature
  2. extractionthe product extracted with diethyl ether (3×75 ml)
  3. dry with materialThe combined organic fractions were dried over sodium sulphate for 16 hrs
  4. filtrationfiltered
  5. customthe solvents removed under reduced pressure
  6. customa rotary evaporator
  7. customto yield a brown oil
  8. distillationThe crude product was distilled under reduced pressure (b.p. 40-°44° C. at 2-3 mm Hg)

Sources & evidence

ORD record
ord-a1dcaa9a7c2f4220b9fc328da916f347
Source dataset
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05814574

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes