4-Hydroxybenzaldehyde → 4-[2-(N-Methyl-N-(2-benzoxazolyl)amino)ethoxy]benzaldehyde

HRID 2119904Notes

Reaction equation

HRID 2119904 reaction equation
[CH3:1][N:2]([CH2:12][CH2:13][OH:14])[C:3]1[O:4][C:5]2[CH:11]=[CH:10][CH:9]=[CH:8][C:6]=2[N:7]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.O[C:35]1[CH:42]=[CH:41][C:38]([CH:39]=[O:40])=[CH:37][CH:36]=1.N(C(OCC)=O)=NC(OCC)=O>O1CCCC1>[CH3:1][N:2]([CH2:12][CH2:13][O:14][C:35]1[CH:42]=[CH:41][C:38]([CH:39]=[O:40])=[CH:37][CH:36]=1)[C:3]1[O:4][C:5]2[CH:11]=[CH:10][CH:9]=[CH:8][C:6]=2[N:7]=1

Participants

6

Reactant 4

HCID 1264-HydroxybenzaldehydeHCID 11776TriphenylphosphineHCID 220568ethyl N-ethoxycarbonyliminocarbamateHCID 102416632-(Benzooxazol-2-yl-methyl-amino)-ethanol

Product 1

HCID 100402134-[2-(N-Methyl-N-(2-benzoxazolyl)amino)ethoxy]benzaldehyde

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Procedure

To a solution of 2-[N-methyl-N-(2-benzoxazolyl) amino]ethanol (9.6 g), triphenylphosphine (13.1 g) and 4-hydroxybenzaldehyde (6.1 g) in dry tetrahydrofuran (150 ml) was added dropwise a solution of diethyl azodicarboxylate (9.0 g) in dry tetrahydrofuran (30 ml), under a blanket of nitrogen with stirring at room temperature. The solution was stirred overnight at room temperature following which the solvent was removed under reduced pressure. The residue was dissolved in diethyl ether (300 ml), filtered and the ether solution was washed with dilute sodium hydroxide solution (200 ml), saturated brine (200 ml), dried (MgSO4), filtered and the solvent evaporated. The title compound (mp 97-98° C.) was obtained after chromatography on silica-gel, eluting with dichloromethane.

Workup

  1. stirringThe solution was stirred overnight at room temperature
  2. customwas removed under reduced pressure
  3. dissolutionThe residue was dissolved in diethyl ether (300 ml)
  4. filtrationfiltered
  5. washthe ether solution was washed with dilute sodium hydroxide solution (200 ml), saturated brine (200 ml)
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. customthe solvent evaporated

Sources & evidence

ORD record
ord-513fae0586d747cc9a7a7b1a8f6510ff
Source dataset
uspto-grants-2004_02
Patent number
US06686475B2

Reaction notes

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