Vanillin → Veratraldehyde

HRID 1262705Notes

Reaction equation

HRID 1262705 reaction equation
[O:1]=[CH:2][C:3]1[CH:11]=[CH:10][C:8]([OH:9])=[C:5]([O:6][CH3:7])[CH:4]=1.[C:12](=O)([O-])[O-].[K+].[K+].C(=O)([O-])[O-].P(OC)(OC)(OC)=O>O>[CH:2](=[O:1])[C:3]1[CH:11]=[CH:10][C:8]([O:9][CH3:12])=[C:5]([O:6][CH3:7])[CH:4]=1

Participants

6

Conditions

Temperature
85 °C

Procedure

In a three-neck flask (capacity 100 ml) equipped with a mechanical stirrer and reflux condenser, 5.00 g (0.033 mol) of vanillin and 5.00 g (0.036 mol) of anhydrous potassium carbonate were placed and the mixture was heated under a nitrogen atmosphere to 85° C. The mixture was a clear to amber melt of vanillin with carbonate in suspension. To this mixture was added 5.00 ml (0.043 mol) of trimethyl phosphate over about 5 minutes while maintaining the reaction temperature below 125° C. The mixture was maintained at about 80° C. for one hour and then cooled to 40° C. The mixture was poured into 20 ml water and extracted two times with 20 ml of methylene chloride. The combined extracts were dried over anhydrous potassium carbonate, filtered, and concentrated to give 5.4 g (99%) of veratraldehyde as a pale oil.

Workup

  1. customIn a three-neck flask (capacity 100 ml) equipped with a mechanical stirrer
  2. temperaturereflux condenser
  3. temperaturewhile maintaining the reaction temperature below 125° C
  4. temperatureThe mixture was maintained at about 80° C. for one hour
  5. temperaturecooled to 40° C
  6. extractionextracted two times with 20 ml of methylene chloride
  7. dry with materialThe combined extracts were dried over anhydrous potassium carbonate
  8. filtrationfiltered
  9. concentrationconcentrated

Sources & evidence

ORD record
ord-8604db59ae024742a11ac12b7983bd1a
Source dataset
uspto-grants-1984_06
Patent number
US04453004

Reaction notes

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