4-Piperidinol, 1,2,2,6,6-pentamethyl- → HCID 20492431, compound
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]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
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
- additionadded
- temperatureThe solution was heated overnight
- temperatureat reflux temperature
- temperaturecooled
- temperaturethe solution heated
- temperatureat reflux for 5 hours
- temperatureOn cooling the precipitate
- filtrationwas filtered off
- customthe filtrate evaporated in vacuo Treatment of the residue with dilute hydrochloric acid
- extractionbasification with dilute sodium hydroxide to a pH 10 was followed by extraction with ether
- customEvaporation
- customafforded a pale yellow oil which
- 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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