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Potassium Carbonate → 1-Ethyl-3-ethynylbenzene

HRID 2240980
Notes
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Reaction equation

HRID 2240980 reaction equation
[CH2:1]([C:3]1[CH:4]=[C:5]([C:9]#[C:10][Si](C)(C)C)[CH:6]=[CH:7][CH:8]=1)[CH3:2].C(=O)([O-])[O-].[K+].[K+]>CO>[CH2:9]([C:5]1[CH:6]=[CH:7][CH:8]=[C:3]([C:1]#[CH:2])[CH:4]=1)[CH3:10]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 11430Potassium CarbonateHCID 67539193HCID 67539193, compound

Product 1

HCID 133018331-Ethyl-3-ethynylbenzeneYield 110%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Conditions

Temperature
25 °C

Procedure

In a 100 mL round-bottomed flask was placed ((3-ethylphenyl)ethynyl)trimethylsilane (3.17 g, 15.66 mmol) and MeOH (31.3 ml) was added to give a yellow solution. Potassium carbonate (21.65 g, 157 mmol) was added and reaction stirred at 25° C. for 1 h. The reaction was partitioned between water (200 mL) and hexanes (200 mL). The organic was washed with water (100 mL) and brine (100 mL). The organic was dried over Na2SO4. The solvent was removed providing 1-ethyl-3-ethynylbenzene (2.24 g, 17.21 mmol, 110% yield) as a dark brown oil that was used as is without further purification.

Workup

  1. customIn a 100 mL round-bottomed flask was placed
  2. customto give a yellow solution
  3. customreaction
  4. customThe reaction was partitioned between water (200 mL) and hexanes (200 mL)
  5. washThe organic was washed with water (100 mL) and brine (100 mL)
  6. dry with materialThe organic was dried over Na2SO4
  7. customThe solvent was removed

Sources & evidence

ORD record
ord-780c1fb33ccd4ad8861e454496d62424
Source dataset
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07723368B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes