Hydrochloric Acid → 5-Formyl-2-methoxybenzoic acid

HRID 1583029Notes

Reaction equation

HRID 1583029 reaction equation
[OH-].[Li+].[CH3:3][O:4][C:5]1[CH:14]=[CH:13][C:12]([CH:15]=[O:16])=[CH:11][C:6]=1[C:7]([O:9]C)=[O:8].Cl>O.O1CCCC1.CO>[CH3:3][O:4][C:5]1[CH:14]=[CH:13][C:12]([CH:15]=[O:16])=[CH:11][C:6]=1[C:7]([OH:9])=[O:8]

Participants

7

Procedure

Lithium hydroxide (1.04 g, 0.043 mol, 3 eq) in water (10 mL) was added to a stirred solution of methyl 2-methoxy-5-formylbenzoate (2.8 g, 0.014 mol, 1 eq) in a mixture of tetrahydrofuran (30 mL) and methanol (20 mL). The solution was stirred overnight, acidified to pH 1 with 10% HCl and the organic solvents removed in vacuo. The aqueous solution was extracted with ethyl acetate (100 mL) and the organic solution washed with brine (100 mL), then extracted with saturated aqueous sodium bicarbonate (3×100 mL). The basic solution was washed with ethyl acetate (100 mL), then acidified to pH 1 with 10% HCl and back extracted with dichloromethane (3×100 mL). The organic solution was dried over sodium sulfate and evaporated in vacuo to give a cream coloured powder (2.01 g, 77%). 1H NMR (CDCl3) δ9.99 (s, 1H, O═C—H), 4.14 (s, 3H, CH3).

Workup

  1. customthe organic solvents removed in vacuo
  2. extractionThe aqueous solution was extracted with ethyl acetate (100 mL)
  3. washthe organic solution washed with brine (100 mL)
  4. extractionextracted with saturated aqueous sodium bicarbonate (3×100 mL)
  5. washThe basic solution was washed with ethyl acetate (100 mL)
  6. extractionback extracted with dichloromethane (3×100 mL)
  7. dry with materialThe organic solution was dried over sodium sulfate
  8. customevaporated in vacuo
  9. customto give a cream

Sources & evidence

ORD record
ord-651cbf1855b149588665d62ed2a99753
Source dataset
uspto-grants-2004_05
Patent number
US06740670B2

Reaction notes

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