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1,1-Dichloroethane → 3,5-Dimethyl-1H-pyrrole-2-carbaldehyde

HRID 1270468
Notes
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Reaction equation

HRID 1270468 reaction equation
Cl[CH:2](Cl)[CH3:3].P(Cl)(Cl)(Cl)=[O:6].[CH3:10][C:11]1[NH:12]C=[C:14]([CH3:16])[CH:15]=1>CN(C)C=O>[CH3:10][C:11]1[NH:12][C:2]([CH:3]=[O:6])=[C:14]([CH3:16])[CH:15]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 63651,1-DichloroethaneHCID 24813Phosphorus oxychlorideHCID 395392,4-Dimethylpyrrole

Product 1

HCID 2704653,5-Dimethyl-1H-pyrrole-2-carbaldehydeYield 90%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Conditions

Temperature
0 °C

Procedure

To a solution dimethylformamide (80.4 g) and 1 L of dichloroethane at 0° C. was added phosphorous oxychoride (153.3 g) over a few minutes and the reaction stirred for 1–2 hr at 0° C. 2,4-Dimethylpyrrole (114.6 g) was added dropwise to the above solution at temperature below 5° C. After the addition was complete the reaction was heated and the aqueous layer isolated and saved. The organic layer was extracted again with 300 mL of water and the two aqueous layers combined. The aqueous phase was extracted with 200 mL of dichloroethane and the organic layer discarded. The aqueous phase was cooled to 10° C. and adjusted to pH 10 with 10% sodium hydroxide. The mixture was stirred at 10° C. for 2 hr. The yellow solid was collected by vacuum filtration and washed thoroughly with water. The solid was dried at room temperature under vacuum to give 110.8 g (90% yield of 2,4-dimethyl-5-formylpyrrole.

Workup

  1. additionAfter the addition
  2. temperaturewas heated
  3. customthe aqueous layer isolated
  4. extractionThe organic layer was extracted again with 300 mL of water
  5. extractionThe aqueous phase was extracted with 200 mL of dichloroethane
  6. temperatureThe aqueous phase was cooled to 10° C.
  7. stirringThe mixture was stirred at 10° C. for 2 hr
  8. filtrationThe yellow solid was collected by vacuum filtration
  9. washwashed thoroughly with water
  10. customThe solid was dried at room temperature under vacuum

Sources & evidence

ORD record
ord-9f8363d5f6cd4b83b01790fd80dfb026
Source dataset
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07202265B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes