Vanillin → 4-[(4-Chlorophenyl)methoxy]-3-methoxybenzaldehyde

HRID 1964885Notes

Reaction equation

HRID 1964885 reaction equation
[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][C:3]=1[O:10][CH3:11].[Cl:12][C:13]1[CH:20]=[CH:19][C:16]([CH2:17]Br)=[CH:15][CH:14]=1.C(=O)([O-])[O-].[K+].[K+]>C(#N)C>[Cl:12][C:13]1[CH:20]=[CH:19][C:16]([CH2:17][O:1][C:2]2[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][C:3]=2[O:10][CH3:11])=[CH:15][CH:14]=1

Participants

5

Reactant 3

HCID 1183VanillinHCID 11430Potassium CarbonateHCID 693291-(Bromomethyl)-4-chlorobenzene

Product 1

HCID 7182634-[(4-Chlorophenyl)methoxy]-3-methoxybenzaldehydeYield 93%

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

To 4-hydroxy-3-methoxybenzaldehyde (105, 600.0 mg, 3.94 mmol) and 4-chlorobenzyl bromide (557, 1.20 g, 5.84 mmol) in acetonitrile (6 mL) was added potassium carbonate (0.390 g, 2.82 mmol). The reaction was microwaved on 300 watts, 120° C. for 10 minutes. The reaction was extracted with ethyl acetate and water. The organic layer was washed with brine, dried over magnesium sulfate, filtered and the volatiles removed by evaporation. The desired compound was purified by recrystallization from hexanes to provide 106 (1.01 g, 93%). MS(ESI) [M−H+]−=275.1.

Workup

  1. customThe reaction was microwaved on 300 watts, 120° C. for 10 minutes
  2. extractionThe reaction was extracted with ethyl acetate and water
  3. washThe organic layer was washed with brine
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. customthe volatiles removed by evaporation
  7. customThe desired compound was purified by recrystallization from hexanes

Sources & evidence

ORD record
ord-03b59bf65d734a3690b35fad26ffa541
Source dataset
uspto-grants-2013_04
Patent number
US08415469B2

Reaction notes

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