Potassium Carbonate → HCID 15617492, compound

HRID 2352112Notes

Reaction equation

HRID 2352112 reaction equation
[OH:1][C:2]1[CH:9]=[CH:8][C:7]([O:10][CH3:11])=[CH:6][C:3]=1[CH:4]=[O:5].C(=O)([O-])[O-].[K+].[K+].[CH2:18](Br)[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28]>CN(C)C=O>[CH2:28]([O:1][C:2]1[CH:9]=[CH:8][C:7]([O:10][CH3:11])=[CH:6][C:3]=1[CH:4]=[O:5])[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][CH2:19][CH3:18]

Participants

5

Conditions

Temperature
100 °C

Procedure

A solution of 2-hydroxy-5-methoxybenzaldehyde (10 g, 65.7 mmoles) in 100 ml of sieve-dried dimethylformamide was added freshly-pulverized potassium carbonate (10 g 72.3 mmoles) and undecyl bromide (15 ml, 67.3 mmoles). The reaction mixture was stirred at 100° C. for 1 hour, cooled to room temperature and ten poured into ice-cold water/hexane. The layers were separated and the organic extract was washed with ice-cold 5% sodium hydroxide solution, water and saturated sodium chloride solution. The organic layer was dried with anhydrous magnesium sulfate, treated with charcoal and concentrated in vacuo. The resulting yellow solid was recrystallized from hexane, to give 16.2 g (80%) of the product as a white solid.

Workup

  1. temperaturecooled to room temperature
  2. additionten poured into ice-cold water/hexane
  3. customThe layers were separated
  4. extractionthe organic extract
  5. washwas washed with ice-cold 5% sodium hydroxide solution, water and saturated sodium chloride solution
  6. dry with materialThe organic layer was dried with anhydrous magnesium sulfate
  7. additiontreated with charcoal
  8. concentrationconcentrated in vacuo
  9. customThe resulting yellow solid was recrystallized from hexane

Sources & evidence

ORD record
ord-395b9c27bf944e9f8352d6aef81f9201
Source dataset
uspto-grants-1989_10
Patent number
US04874792

Reaction notes

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