Dimethylformamide → 3,4-Dimethoxynaphthalene-1-carbaldehyde

HRID 479981Notes

Reaction equation

HRID 479981 reaction equation
[CH3:1][O:2][C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH:6]=[CH:5][C:4]=1[O:13][CH3:14].CN([CH:18]=[O:19])C.O=P(Cl)(Cl)Cl>C1C(Cl)=CC=C(Cl)C=1>[CH3:14][O:13][C:4]1[CH:5]=[C:6]([CH:18]=[O:19])[C:7]2[C:12]([C:3]=1[O:2][CH3:1])=[CH:11][CH:10]=[CH:9][CH:8]=2

Participants

5

Reactant 3

HCID 6228DimethylformamideHCID 24813Phosphorus oxychlorideHCID 2992571,2-dimethoxynaphthalene

Product 1

HCID 134955543,4-Dimethoxynaphthalene-1-carbaldehydeYield 68.9%

Reagents, catalysts & solvents 1

HCID 46851,4-DichlorobenzeneSolvent

Conditions

Temperature
0 °C

Procedure

A mixture of 1,2-dimethoxynaphthalene (0.74 g, 4 mmol) and DMF (0.8 mL, 10 mmol) in dichlorobenzene (0.8 mL) was stirred with POCl3 at 100° C. for 2h. The reaction mixture was cooled to 0° C, quenched with a cold aqueous solution of NaOAc, diluted with H2O and extracted with benzene. The extracts were dried (MgSO4), concentrated and in vacuo and dichlorobenzene was removed by kugelrohr distillation at 110° C./0.5 mm Hg. Column chromatography (20%EtOAc in hexane) gave the product 518 (596 mg, 68%), which was used in the following step without further purification. 1H NMR (CDCl3) 10.42 (s, 1H), 9.00-9.15 (m, 1H), 8.15-8.30 (m, 1H), 7.61 (s, 1H), 7.50-7.65 (m, 2H), 4.12 (s, 3H), 4.07 (s, 3H).

Workup

  1. customquenched with a cold aqueous solution of NaOAc
  2. additiondiluted with H2O
  3. extractionextracted with benzene
  4. dry with materialThe extracts were dried (MgSO4)
  5. concentrationconcentrated and in vacuo and dichlorobenzene
  6. customwas removed by kugelrohr distillation at 110° C./0.5 mm Hg

Sources & evidence

ORD record
ord-d83dfd1552f747cca692164be8e462e6
Source dataset
uspto-grants-2003_11
Patent number
US06649587B1

Reaction notes

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