Salicylaldehyde → 2-Undecyloxybenzaldehyde

HRID 568899

Reaction equation

HRID 568899 reaction equation
[H-].[Na+].[CH:3](=[O:11])[C:4]1[C:5](=[CH:7][CH:8]=[CH:9][CH:10]=1)[OH:6].[CH2:12](Br)[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22]>CN(C)C=O.CCCCCC>[CH2:22]([O:6][C:5]1[CH:7]=[CH:8][CH:9]=[CH:10][C:4]=1[CH:3]=[O:11])[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH3:12]

Participants

6

Reactant 3

HCID 6998SalicylaldehydeHCID 127441-BromoundecaneHCID 24758Sodium hydride

Product 1

HCID 156174952-Undecyloxybenzaldehyde

Reagents, catalysts & solvents 2

HCID 6228DimethylformamideSolvent2×HCID 8058HexaneSolvent

Procedure

To a stirred suspension of sodium hydride (10.0 mmoles), which was prewashed with petroleum ether, in sieve dried dimethylformamide (10 ml) was added dropwise a solution of salicylaldehyde (10.1 mmoles) in dimethylformamide (1 ml). To the reaction mixture was then added undecyl bromide (10.0 mmoles) and the mixture stirred for 16 hours at ambient temperature under nitrogen. The reaction mixture was taken up in hexane (50 ml) and washed with 10 percent sodium hydroxide (2×50 ml) and saturated sodium chloride (50 ml). The organic phase was dried over anhydrous magnesium sulfate and charcoal. Evaporation of the volatiles yielded a colorless liquid which was purified by flash chromatography over silica gel with 2 percent ethyl acetate in hexane as eluant to afford the desired product as an oil.

Workup

  1. washwashed with 10 percent sodium hydroxide (2×50 ml) and saturated sodium chloride (50 ml)
  2. dry with materialThe organic phase was dried over anhydrous magnesium sulfate and charcoal
  3. customEvaporation of the volatiles
  4. customyielded a colorless liquid which
  5. customwas purified by flash chromatography over silica gel with 2 percent ethyl acetate in hexane as eluant

Sources & evidence

ORD record
ord-b8010cf9df3547c28754e3a851c51719
Source dataset
uspto-grants-1988_03
Patent number
US04730005

Linked notes

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