Iodoethane → HCID 22498573, compound

HRID 1815519Notes

Reaction equation

HRID 1815519 reaction equation
[CH2:1](I)[CH3:2].[O:4]1[CH:8]=[CH:7][CH:6]=[C:5]1[C:9](=[CH2:13])[C:10]([OH:12])=[O:11].C(N(C(C)C)CC)(C)C>C(#N)C>[O:4]1[CH:8]=[CH:7][CH:6]=[C:5]1[C:9](=[CH2:13])[C:10]([O:12][CH2:1][CH3:2])=[O:11]

Participants

5

Conditions

Temperature
60 °C

Procedure

Ethyl iodide (64 mL, 0.796 mol) was added to furylacrylic acid (100 g, 0.724 mol), diisopropylethyl amine (140 mL, 0.796 mmol), in acetonitrile (1100 mL), and the mixture was heated to 60° C. After 18 h, the dark solution was cooled to room temperature and concentrated in vacuo. The resulting brown sludge was diluted with Et2O (500 mL), washed with 1 N aqueous HCl (2×250 mL), washed with 0.2 N aqueous NaOH (2×250 mL), washed with saturated aqueous NaHCO3 (1×250 mL), dried (MgSO4), filtered, and concentrated to a black oil (114 g, 95%). 1H NMR (DMSO-d6, 300 MHz) δ 7.84 (d, J=1.7 Hz, 1H), 7.46 (d, J=15.6 Hz, 1H), 6.97 (d, J=3.4 Hz, 1H), 6.33 (dd, J=3.4 Hz, J=1.7 Hz, 1H), 6.22 (d, J=15.9 Hz, 1H), 4.17 (q, J=7.1 Hz, 2H), 1.24 (t, J=7.1 Hz, 3H); MS (APCI) m/z 167 (M+H)+.

Workup

  1. temperaturethe dark solution was cooled to room temperature
  2. concentrationconcentrated in vacuo
  3. additionThe resulting brown sludge was diluted with Et2O (500 mL)
  4. washwashed with 1 N aqueous HCl (2×250 mL)
  5. washwashed with 0.2 N aqueous NaOH (2×250 mL)
  6. washwashed with saturated aqueous NaHCO3 (1×250 mL)
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered
  9. concentrationconcentrated to a black oil (114 g, 95%)

Sources & evidence

ORD record
ord-b7b2004d9eed490f8cbfe4d428614dad
Source dataset
uspto-grants-2005_04
Patent number
US06878700B1

Reaction notes

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