Sodium Carbonate → 3-Propyl-benzofuran

HRID 1362316Notes

Reaction equation

HRID 1362316 reaction equation
[CH2:1]([O:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1I)[CH:2]=[CH:3][CH3:4].[C:13]([O-])([O-])=O.[Na+].[Na+].CC([O-])=O.[Na+]>CN(C=O)C.[N+](CCCC)(CCCC)(CCCC)CCCC.[Cl-].CCOC(C)=O.CC([O-])=O.CC([O-])=O.[Pd+2]>[CH2:3]([C:2]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[O:5][CH:1]=1)[CH2:4][CH3:13]

Participants

8

Procedure

To a solution of 1-but-2-enyloxy-iodobenzene (4.00 g, 13.8 mmol) in DMF (46 mL) was added n-Bu4NCl (5.36 g. 19.3 mmol), Pd(OAc)2 (0.168 g, 0.690 mmol), Na2CO3 (2.99 g, 28.2 mmol) and NaOAc (1.13 g, 13.8 mmol). The mixture was heated to reflux under nitrogen atmosphere overnight. The mixture was diluted with EtOAc and washed with water. The aqueous layer was extracted with EtOAc (3×). The combined organics were washed with brine and dried over Na2SO4. Purification by column chromatography (silica gel, hexanes) gave the title compound (1.79 g, 81%) as a yellow oil: 1H NMR (300 MHz, DMSO-d6) δ 7.75 (s, 1H), 7.63-7.60 (m, 1H), 7.54 (d, J=7.5 Hz, 1H), 7.33-7.22 (m, 2H), 2.64-2.59 (m, 2H), 1.72-1.64 (m, 2H), 0.96 (t, J=7.2 Hz, 3H); ESI MS m/z 161 (M+H)+.

Workup

  1. temperatureThe mixture was heated
  2. temperatureto reflux under nitrogen atmosphere overnight
  3. washwashed with water
  4. extractionThe aqueous layer was extracted with EtOAc (3×)
  5. washThe combined organics were washed with brine
  6. dry with materialdried over Na2SO4
  7. customPurification by column chromatography (silica gel, hexanes)

Sources & evidence

ORD record
ord-b739fbe551fb4bbe9c23f922d1411eaa
Source dataset
uspto-grants-2011_02
Patent number
US07879872B2

Reaction notes

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