Water → HCID 15572314, compound

HRID 2286582Notes

Reaction equation

HRID 2286582 reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].[C:7]1([C:13]2[C:14]([C:24](OCC)=O)=[CH:15][NH:16][C:17]=2[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.O.[OH-].[Na+]>C1COCC1>[C:7]1([C:13]2[C:14]([CH3:24])=[CH:15][NH:16][C:17]=2[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1

Participants

6

Reactant 4

HCID 962Water2×HCID 14798Sodium HydroxideHCID 10379523HCID 10379523, compoundHCID 21226445Aluminium lithium hydride

Product 1

HCID 15572314HCID 15572314, compoundYield 53.8%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Procedure

To a stirred slurry of 0.76 g (20 m moles) of lithium aluminum hydride in 25 ml. THF was added dropwise a solution of 0.58 g (2 m moles) of ethyl 4,5-diphenylpyrrole-3-carboxylate in 5 ml THF. The mixture was heated at reflux overnight. After cooling, 0.8 ml water, 2.4 ml 15% sodium hydroxide solution and 0.8 ml water were added dropwise. The solids were removed by filtration and the filtrate concentrated by rotary evaporation. The crystalline residue was purified by chromatography on 50 g Silic AR CC-7, eluting with hexane/toluene (90/10) to give 0.25 g of product, m.p. 163°-4°.

Workup

  1. temperatureThe mixture was heated
  2. temperatureat reflux overnight
  3. temperatureAfter cooling
  4. customThe solids were removed by filtration
  5. concentrationthe filtrate concentrated by rotary evaporation
  6. customThe crystalline residue was purified by chromatography on 50 g Silic AR CC-7
  7. washeluting with hexane/toluene (90/10)

Sources & evidence

ORD record
ord-830f0ab7ceef4aa594130fe8f17ac74e
Source dataset
uspto-grants-1981_05
Patent number
US04267184

Reaction notes

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