4-Hydroxybenzaldehyde → 4-(3-(Diethylamino)propoxy)benzaldehyde

HRID 17651

Reaction equation

HRID 17651 reaction equation
[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][CH:3]=1.C([O-])([O-])=O.[Cs+].[Cs+].S([O-])(=O)(=O)C.[CH2:21]([N:23]([CH2:28][CH3:29])[CH2:24][CH2:25][CH2:26]O)[CH3:22].CS(Cl)(=O)=O>CS(C)=O>[CH2:21]([N:23]([CH2:28][CH3:29])[CH2:24][CH2:25][CH2:26][O:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][CH:3]=1)[CH3:22]

Participants

7

Conditions

Temperature
90 °C

Procedure

To a stirred solution of 4-hydroxybenzaldehyde (20 mmol) in DMSO (80 mL) at rt, solid Cs2CO3 (50 mmol) was added. The mesylate prepared from 3-diethylamino-1-propanol and methanesulfonyl chloride, General Procedure P2 (30 mmol) was added to the reaction mixture and heated to 90° C. until the reaction was complete. After cooling to rt, the reaction was quenched by cold H2O (100 mL), and the resulting mixture was extracted with EtOAc (3×100 mL). The combined EtOAc extracts were washed with brine (3×50 mL) and dried (anhydrous Na2SO4). The solvent was removed in vacuo, and the crude product was purified by silica gel column chromatography (eluting with 10% MeOH in DCM+0.5% Et3N) to afford 4-(3-diethylaminopropoxy)benzaldehyde.

Workup

  1. additionwas added to the reaction mixture
  2. temperatureAfter cooling to rt
  3. customthe reaction was quenched by cold H2O (100 mL)
  4. extractionthe resulting mixture was extracted with EtOAc (3×100 mL)
  5. washThe combined EtOAc extracts were washed with brine (3×50 mL)
  6. dry with materialdried (anhydrous Na2SO4)
  7. customThe solvent was removed in vacuo
  8. customthe crude product was purified by silica gel column chromatography (eluting with 10% MeOH in DCM+0.5% Et3N)

Sources & evidence

ORD record
ord-db5bf796934549268433edbace0a4a79
Source dataset
uspto-grants-2010_06
Patent number
US07737285B2

Linked notes

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