Water → HCID 56626090, compound

HRID 1633107Notes

Reaction equation

HRID 1633107 reaction equation
[CH2:1]([Li])CCC.[CH2:6]1[O:16][CH:9]([CH2:10][CH2:11][CH2:12][CH2:13][C:14]#C)[O:8][CH2:7]1.[C:17]([C:21]1[CH:28]=[CH:27][C:24]([CH:25]=[O:26])=[CH:23][CH:22]=1)([O:19][CH3:20])=[O:18].O>CCOCC>[CH2:7]1[O:8][C:9]([CH3:1])([CH2:10][CH2:11][CH2:12][C:13]#[C:14][CH:25]([C:24]2[CH:27]=[CH:28][C:21]([C:17]([O:19][CH3:20])=[O:18])=[CH:22][CH:23]=2)[OH:26])[O:16][CH2:6]1

Participants

6

Procedure

n-Butyl-lithium (1 equivalent) was added dropwise under nitrogen to a solution of heptan-1-yne-7-one ethylene ketal (5.0 g) in ether at ice salt temperature and gave an intense red colour. The solution was stirred at this temperature for 40 minutes. This solution was added to a solution of 4-carbomethoxybenzaldehyde (5.3 g) at the same temperature and produced a grey precipitate. The mixture was left to warm to room temperature. Water was added, the layers separated and the ether layer dried (MgSO4). Removal of the solvent gave an oil which was chromatographed on silica (300 g). Elution with ether gave 1-(4-carbomethoxyphenyl)-1-hydroxyoctan-2-yne-7-one ethylene ketal as a clear oil (5 g). τ (CDCl3) 8.77 (3H, s), 8.35 (4H, m), 7.75 (2H, t, J=7 Hz), 6.85 (1H, broad), 6.16 (3H, s+4H, s), 4.52 (1H, s), 2.45 (2H, d, J=8 Hz), 2.0 (2H, d, J=8 Hz).

Workup

  1. customgave an intense red colour
  2. customproduced a grey precipitate
  3. waitThe mixture was left
  4. customthe layers separated
  5. dry with materialthe ether layer dried (MgSO4)
  6. customRemoval of the solvent
  7. customgave an oil which
  8. customwas chromatographed on silica (300 g)
  9. washElution with ether

Sources & evidence

ORD record
ord-e422019ff919400bac4867250b620f6c
Source dataset
uspto-grants-1984_10
Patent number
US04478849

Reaction notes

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