3-(3-(1,3-Dioxoisoindolin-2-yl)propyl)benzaldehyde → HCID 68938969, compound

HRID 1967685Notes

Reaction equation

HRID 1967685 reaction equation
[Br-].[CH3:2][O:3][C:4]1[CH:29]=[CH:28][CH:27]=[C:26]([O:30][CH3:31])[C:5]=1[CH2:6][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[O:32]=[C:33]1[C:41]2[C:36](=[CH:37][CH:38]=[CH:39][CH:40]=2)[C:35](=[O:42])[N:34]1[CH2:43][CH2:44][CH2:45][C:46]1[CH:47]=[C:48]([CH:51]=[CH:52][CH:53]=1)[CH:49]=O>>[CH3:31][O:30][C:26]1[CH:27]=[CH:28][CH:29]=[C:4]([O:3][CH3:2])[C:5]=1/[CH:6]=[CH:49]/[C:48]1[CH:47]=[C:46]([CH2:45][CH2:44][CH2:43][N:34]2[C:35](=[O:42])[C:36]3[C:41](=[CH:40][CH:39]=[CH:38][CH:37]=3)[C:33]2=[O:32])[CH:53]=[CH:52][CH:51]=1

Participants

3

Reactant 2

HCID 577664653-(3-(1,3-Dioxoisoindolin-2-yl)propyl)benzaldehydeHCID 86632153HCID 86632153, compound

Product 1

HCID 68938969HCID 68938969, compound

Procedure

2,6-Dimethoxybenzyltriphenylphosphonium bromide was coupled with phthalimide 29 following the method used in Example 44, except that the reaction was stirred overnight after warming up to room temperature. After concentration under reduced pressure, the residue was partitioned between EtOAc and water. The combined organics were washed with brine, dried over MgSO4 and concentrated under reduced pressure. Purification by flash chromatography (7 to 60% EtOAc-hexanes gradient) gave (E)-2-(3-(3-(2,6-dimethoxystyryl)phenyl)propyl)isoindoline-1,3-dione as a light yellow oil. Yield (0.317 g, 82%): 1H NMR (400 MHz, DMSO-d6) δ 7.79-7.84 (m, 4H), 7.42 (d, J=17.2 Hz, 1H), 7.17-7.32 (m, 5H), 7.06-7.09 (m, 1H), 6.58 (d, J=8.4 Hz, 2H), 3.83 (s, 6H), 3.61 (t, J=7.2 Hz, 2H), 2.63 (t, J=8.0 Hz, 2H), 1.88-1.96 (m, 2H).

Workup

  1. concentrationAfter concentration under reduced pressure
  2. customthe residue was partitioned between EtOAc and water
  3. washThe combined organics were washed with brine
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated under reduced pressure
  6. customPurification by flash chromatography (7 to 60% EtOAc-hexanes gradient)

Sources & evidence

ORD record
ord-7cb1c18d66a84c368c6c900277bcf331
Source dataset
uspto-grants-2013_04
Patent number
US08420863B2

Reaction notes

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