Sodium Carbonate → HCID 21436092, compound

HRID 328250Notes

Reaction equation

HRID 328250 reaction equation
[C:1]1([C:7]2([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[CH2:12][CH2:11][NH:10][CH2:9][CH2:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[F:19][C:20]1[CH:31]=[CH:30][C:23]([C:24]([CH2:26][CH2:27][CH2:28]I)=[O:25])=[CH:22][CH:21]=1.C(=O)([O-])[O-].[Na+].[Na+]>C(C(C)=O)C>[F:19][C:20]1[CH:21]=[CH:22][C:23]([C:24]([CH2:26][CH2:27][CH2:28][N:10]2[CH2:9][CH2:8][C:7]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)[CH2:12][CH2:11]2)=[O:25])=[CH:30][CH:31]=1

Participants

5

Procedure

6.1 g. of 4,4-diphenylpiperidine are heated to boiling with 6.2 g. of 3-(p-fluorobenzoyl)propyl iodide and 5.3 g of anhydrous sodium carbonate in 30 cc. of methyl ethyl ketone for 8 hours while stirring. After cooling, the precipitated salt is filtered off and the filtrate is evaporated to dryness. The residue is dissolved in water and the aqueous solution is rendered alkaline by the addition of sodium hydroxide solution. The resulting base is recovered by repeated extraction with ether. The combined ether extracts are dried over potassium carbonate, the ether is distilled off, and the residue is recrystallized from ethanol with the addition of activated charcoal. Thereby, 9 g. of 1-[3-(p-fluorobenzoyl)propyl] -4,4-diphenylpiperidine of the melting point 107° to 108° C. are obtained. On adding fumaric acid to its solution in ether, the furmarate of the melting point 195° to 197° C. is obtained.

Workup

  1. temperatureAfter cooling
  2. filtrationthe precipitated salt is filtered off
  3. customthe filtrate is evaporated to dryness
  4. dissolutionThe residue is dissolved in water
  5. additionby the addition of sodium hydroxide solution
  6. customThe resulting base is recovered
  7. extractionextraction with ether
  8. dry with materialThe combined ether extracts are dried over potassium carbonate
  9. distillationthe ether is distilled off
  10. customthe residue is recrystallized from ethanol with the addition of activated charcoal

Sources & evidence

ORD record
ord-802a1e58393c4759b50086142fcb2ab3
Source dataset
uspto-grants-1977_04
Patent number
US04016280

Reaction notes

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