Ethyl 4-[(2,6-dimethylphenyl)imino]-1-piperidinecarboxylate → HCID 23338990, compound

HRID 2049352Notes

Reaction equation

HRID 2049352 reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[N:9]=[C:10]1[CH2:15][CH2:14][N:13]([C:16]([O:18][CH2:19][CH3:20])=[O:17])[CH2:12][CH2:11]1.[H][H]>[Pt](=O)=O.CO>[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[NH:9][CH:10]1[CH2:15][CH2:14][N:13]([C:16]([O:18][CH2:19][CH3:20])=[O:17])[CH2:12][CH2:11]1

Participants

5

Reactant 2

HCID 23339012Ethyl 4-[(2,6-dimethylphenyl)imino]-1-piperidinecarboxylateHCID 178418361HCID 178418361, compound

Product 1

HCID 23338990HCID 23338990, compound

Reagents, catalysts & solvents 2

HCID 345198Adams' catalystCatalystHCID 887MethanolSolvent

Procedure

A mixture of 45 parts of ethyl 4-[(2,6-dimethylphenyl)imino]-1-piperidinecarboxylate, 0.3 parts of platinum dioxide in 160 parts of methanol is hydrogenated at normal pressure and at a temperature between 24° and 35° C. After the calculated amount of hydrogen is taken up, hydrogenation is stopped. The catalyst is filtered off and the filtrate is evaporated. The oily residue is distilled, to yield 30 parts of the oily free base of ethyl 4-[(2,6-dimethylphenyl)amino]-1-piperidinecarboxylate; bp. 148°-153° C. at 0.01 mm. pressure. From this distillate, the hydrochloride salt is prepared in the usual manner in 1,1'-oxybisethane. The precipitated solid salt is filtered off and dried, yielding 28.5 parts of ethyl 4-[(2,6-dimethylphenyl)amino]-1-piperidinecarboxylate hydrochloride; mp. 195.5° C.

Workup

  1. customis hydrogenated at normal pressure and at a temperature between 24° and 35° C
  2. filtrationThe catalyst is filtered off
  3. customthe filtrate is evaporated
  4. distillationThe oily residue is distilled

Sources & evidence

ORD record
ord-1d422df6e2bc4f2da8b1b36fe7a71283
Source dataset
uspto-grants-1980_04
Patent number
US04197304

Reaction notes

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