4-Piperidinol, 1,2,2,6,6-pentamethyl- → HCID 20492431, compound

HRID 434455Notes

Reaction equation

HRID 434455 reaction equation
[CH3:1][N:2]1[C:7]([CH3:9])([CH3:8])[CH2:6][CH:5]([OH:10])[CH2:4][C:3]1([CH3:12])[CH3:11].S(O[CH2:24][CH2:25][O:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)(C1C=CC(C)=CC=1)(=O)=O>[Na]>[O:26]([CH2:25][CH2:24][O:10][CH:5]1[CH2:6][C:7]([CH3:8])([CH3:9])[N:2]([CH3:1])[C:3]([CH3:12])([CH3:11])[CH2:4]1)[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1

Participants

4

Procedure

30 parts of 1,2,2,6,6,-pentamethylpiperidin-4-ol were dissolved in 250 parts of sodium added. The solution was heated overnight at reflux temperature and then cooled. 38 parts of 2-phenoxyethanol tosylate were added dropwise and the solution heated at reflux for 5 hours. On cooling the precipitate was filtered off and the filtrate evaporated in vacuo Treatment of the residue with dilute hydrochloric acid and then basification with dilute sodium hydroxide to a pH 10 was followed by extraction with ether. Evaporation afforded a pale yellow oil which was chromatographed on aluminum to give 4-(2'-phenoxyethoxy)-1,2,2,6,6-pentamethylpiperidine as a colourless oil which gave the following elemental analysis by weight:

Workup

  1. additionadded
  2. temperatureThe solution was heated overnight
  3. temperatureat reflux temperature
  4. temperaturecooled
  5. temperaturethe solution heated
  6. temperatureat reflux for 5 hours
  7. temperatureOn cooling the precipitate
  8. filtrationwas filtered off
  9. customthe filtrate evaporated in vacuo Treatment of the residue with dilute hydrochloric acid
  10. extractionbasification with dilute sodium hydroxide to a pH 10 was followed by extraction with ether
  11. customEvaporation
  12. customafforded a pale yellow oil which
  13. customwas chromatographed on aluminum

Sources & evidence

ORD record
ord-5c3dfd647caf47a79ba1949c3735203c
Source dataset
uspto-grants-1983_08
Patent number
USRE031343

Reaction notes

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