Acetic Anhydride → 2-Hydroxymethyl-4-(4-methoxybutoxy)pyridine

HRID 357570Notes

Reaction equation

HRID 357570 reaction equation
[CH3:1][O:2][CH2:3][CH2:4][CH2:5][CH2:6][O:7][C:8]1[CH:13]=[CH:12][N+:11]([O-])=[C:10]([CH3:15])[CH:9]=1.C(OC(=O)C)(=[O:18])C>>[OH:18][CH2:15][C:10]1[CH:9]=[C:8]([O:7][CH2:6][CH2:5][CH2:4][CH2:3][O:2][CH3:1])[CH:13]=[CH:12][N:11]=1

Participants

3

Conditions

Temperature
100 °C

Procedure

5.06 g (0.024 mol) of 4-(4-methoxybutoxy)-2-methylpyridine 1-oxide was dissolved in 80 ml of acetic anhydride to obtain a solution. This solution was stirred at 100° C. for one hour, cooled and distilled to remove the solvent. 150 ml of 1N hydrochloric acid was added to the residue. The obtained mixture was stirred at 100° C. for one hour, cooled, neutralized with sodium hydrogencarbonate and extracted with 200 ml of chloroform twice. The extract was dried over magnesium sulfate and filtered. The filtrate was distilled to remove the solvent and the residue was dried in a vacuum to obtain 5.66 g of the title compound as a crude oil.

Workup

  1. customto obtain a solution
  2. temperaturecooled
  3. distillationdistilled
  4. customto remove the solvent
  5. addition150 ml of 1N hydrochloric acid was added to the residue
  6. stirringThe obtained mixture was stirred at 100° C. for one hour
  7. temperaturecooled
  8. extractionextracted with 200 ml of chloroform twice
  9. dry with materialThe extract was dried over magnesium sulfate
  10. filtrationfiltered
  11. distillationThe filtrate was distilled
  12. customto remove the solvent
  13. customthe residue was dried in a vacuum

Sources & evidence

ORD record
ord-033d0e02aecf4e8db5c0fcb3e97bad9c
Source dataset
uspto-grants-1998_11
Patent number
US05840910

Reaction notes

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