Hydrochloric Acid → 3-[4-(1,1-Dimethylheptyl)-2-hydroxyphenyl]-1-N-methylpiperidine

HRID 2166625Notes

Reaction equation

HRID 2166625 reaction equation
[CH3:1][C:2]([C:10]1[CH:15]=[CH:14][C:13]([CH:16]2[CH2:21][CH2:20][CH2:19][NH:18][CH2:17]2)=[C:12]([OH:22])[CH:11]=1)([CH3:9])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[CH2:23]=O.Cl.[H][H]>[Pd]>[CH3:9][C:2]([C:10]1[CH:15]=[CH:14][C:13]([CH:16]2[CH2:21][CH2:20][CH2:19][N:18]([CH3:23])[CH2:17]2)=[C:12]([OH:22])[CH:11]=1)([CH3:1])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]

Participants

6

Reactant 4

HCID 313Hydrochloric AcidHCID 712FormaldehydeHCID 155715583-[4-(1,1-Dimethylheptyl)-2-hydroxyphenyl]piperidineHCID 178418361HCID 178418361, compound

Product 1

HCID 155715603-[4-(1,1-Dimethylheptyl)-2-hydroxyphenyl]-1-N-methylpiperidineYield 90%

Reagents, catalysts & solvents 1

HCID 23938PalladiumCatalyst

Procedure

A mixture of 600 mg. (1.98 mmoles) of 3-[4-(1,1-dimethylheptyl)-2-hydroxyphenyl]-piperidine, 0.78 ml. of 37% formaldehyde, 1.98 ml. of 1 N hydrochloric acid and 150 mg. of 5% palladium-on-carbon is hydrogenated under 55 p.s.i. of hydrogen for 1.5 hours. The reaction mixture is filtered through diatomaceous earth and concentrated under reduced pressure. The residue is diluted with 75 ml. of saturated sodium bicarbonate and extracted with two 75 ml. portions of dichloromethane. The combined extract is washed with 75 ml. of saturated sodium chloride, dried over magnesium sulfate and evaporated to yield 567 mg. (90%) of the title compound as an oil.

Workup

  1. additionA mixture of 600 mg
  2. filtrationThe reaction mixture is filtered through diatomaceous earth
  3. concentrationconcentrated under reduced pressure
  4. additionThe residue is diluted with 75 ml
  5. extractionof saturated sodium bicarbonate and extracted with two 75 ml
  6. extractionThe combined extract
  7. washis washed with 75 ml
  8. dry with materialof saturated sodium chloride, dried over magnesium sulfate
  9. customevaporated
  10. customto yield 567 mg

Sources & evidence

ORD record
ord-f562cf8fd9e2443b8ae35db9a0ae856b
Source dataset
uspto-grants-1983_06
Patent number
US04387229

Reaction notes

Loading…