Water → 5-Cyclopenten-1-ylpyridine-3-carboxaldehyde

HRID 1373994Notes

Reaction equation

HRID 1373994 reaction equation
Br[C:2]1[CH:3]=[N:4][CH:5]=[C:6]([C:8]2[CH2:12][CH2:11][CH2:10][CH:9]=2)[CH:7]=1.C([Li])CCC.N1(C=O)CC[O:21][CH2:20]C1.O>CCOCC>[C:8]1([C:6]2[CH:7]=[C:2]([CH:20]=[O:21])[CH:3]=[N:4][CH:5]=2)[CH2:12][CH2:11][CH2:10][CH:9]=1

Participants

6

Conditions

Temperature
-60 °C

Procedure

A solution of 3-bromo-5-cyclopenten-1-ylpyridine (9) (1 g, 4.5 mmol) in 25 ml of ether is added to a solution of n-butyllithium (1.6M in hexane, 4.2 ml, 6.7 mmol) in 25 ml of ether kept at −60° C. The reaction mixture is stirred for 2 h 30 min at −60° C. and then 1.4 ml of 4-morpholinecarboxaldehyde (13.4 mmol) are added. The reaction is stirred for 1 hour at −60° C. and then poured into water, the organic phase is washed with a saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue is purified by flash chromatography on silica gel (cyclohexane/ethyl acetate: 80/20). The title product is obtained in the form of a beige solid (0.38 g).

Workup

  1. customkept at −60° C
  2. stirringThe reaction is stirred for 1 hour at −60° C.
  3. washthe organic phase is washed with a saturated aqueous sodium chloride solution
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customThe residue is purified by flash chromatography on silica gel (cyclohexane/ethyl acetate: 80/20)

Sources & evidence

ORD record
ord-762401b28d6447b18fb35e53035c8bf9
Source dataset
uspto-grants-2007_01
Patent number
US07163957B2

Reaction notes

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