Sodium borohydride → HCID 23338998, compound

HRID 2049592Notes

Reaction equation

HRID 2049592 reaction equation
[CH3:1][CH:2]([N:4]1[CH2:9][CH2:8][C:7](=[N:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH2:6][CH2:5]1)[CH3:3].[BH4-].[Na+]>CO>[CH3:3][CH:2]([N:4]1[CH2:9][CH2:8][CH:7]([NH:10][C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH2:6][CH2:5]1)[CH3:1]

Participants

4

Reactant 2

HCID 4311764Sodium borohydrideHCID 23339073HCID 23339073, compound

Product 1

HCID 23338998HCID 23338998, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

To a stirred and warmed (30°-40° C.) solution of 72 parts of N-[1-(1-methylethyl)-4-piperidinylidene]benzenamine in 480 parts of methanol are added portionwise20 parts of sodium borohydride. Upon completion, stirring is continued overnight at at room temperature. The reaction mixture is evaporated and the residue is dissolved in water. The solution is extracted with 4-methyl-2-pentanone. The extract is washed with water and acidified with a diluted hydrochloric acid solution. The aqueous acid phase is alkalized with a diluted sodium hydroxide solution till pH 9 and the product is extracted with 4-methyl-2-pentanone. The extract is washed with water, dried, filtered and evaporated. The residue is distilled (bp. 135°-140° C. at 0.2 mm. pressure) and the distillate is crystallized from petroleumether, yielding 21 parts of 1-(1-methylethyl)-N-phenyl-4-piperidinamine; mp. 69.3° C.

Workup

  1. stirringUpon completion, stirring
  2. customThe reaction mixture is evaporated
  3. dissolutionthe residue is dissolved in water
  4. extractionThe solution is extracted with 4-methyl-2-pentanone
  5. washThe extract is washed with water
  6. extractionthe product is extracted with 4-methyl-2-pentanone
  7. washThe extract is washed with water
  8. customdried
  9. filtrationfiltered
  10. customevaporated
  11. distillationThe residue is distilled (bp. 135°-140° C. at 0.2 mm. pressure)
  12. customthe distillate is crystallized from petroleumether

Sources & evidence

ORD record
ord-a95ae38ba88244ffafb4bd2fea48b374
Source dataset
uspto-grants-1980_04
Patent number
US04198411

Reaction notes

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