Methyl 4-Formylbenzoate → HCID 22282641, compound

HRID 1583054Notes

Reaction equation

HRID 1583054 reaction equation
Br[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=[C:4]([CH3:12])[CH:3]=1.[Li]CCCC.[CH:18]([C:20]1[CH:29]=[CH:28][C:23]([C:24]([O:26][CH3:27])=[O:25])=[CH:22][CH:21]=1)=[O:19].[Li]>C1COCC1>[OH:19][CH:18]([C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=[C:4]([CH3:12])[CH:3]=1)[C:20]1[CH:21]=[CH:22][C:23]([C:24]([O:26][CH3:27])=[O:25])=[CH:28][CH:29]=1

Participants

6

Conditions

Temperature
-78 °C

Procedure

4-Bromo-2-methylquinoline (401a) (1.0 g, 4.5 mmol) was dissolved in 10 mL of anhydrous THF and the resulting solution was cooled down to −78° C. A solution of n-BuLi (3.0 mL, 1.6M, 4.8 mmol) was added slowly and the resulting solution was maintained at −78° C. for 5 min. Meanwhile, in another flask methyl 4-formylbenzoate (0.9 g, 5.4 mmol) was dissolved in 20 mL of anhydrous THF and the resulting solution was cooled to −78° C. before the lithium reagent made above was cannulated. The whole mixture was stirred for 30 min before quenched with MeOH. The solution was then diluted with ethyl acetate and washed with H2O and brine. After dried over MgSO4, the organic solution was filtered and concentrated. The residue was purified on silica gel to provide methyl 4-[hydroxy(2-methyl-4-quinolinyl)methyl]benzoate (0.9 g, 65%). MS (AP+): 308 (M+1).

Workup

  1. temperaturethe resulting solution was maintained at −78° C. for 5 min
  2. custombefore quenched with MeOH
  3. additionThe solution was then diluted with ethyl acetate
  4. washwashed with H2O and brine
  5. dry with materialAfter dried over MgSO4
  6. filtrationthe organic solution was filtered
  7. concentrationconcentrated
  8. customThe residue was purified on silica gel

Sources & evidence

ORD record
ord-27b776f654134cf89ed6292ca50a9f3a
Source dataset
uspto-grants-2004_05
Patent number
US06740649B2

Reaction notes

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