Sodium Iodide → 2-Propenoic acid, 3-iodo-, 1-methylethyl ester, (2Z)-

HRID 1500383Notes

Reaction equation

HRID 1500383 reaction equation
[C:1]([O:5][CH:6]([CH3:8])[CH3:7])(=[O:4])[C:2]#[CH:3].[Na+].[I-:10]>CC(O)=O>[I:10]/[CH:3]=[CH:2]\[C:1]([O:5][CH:6]([CH3:8])[CH3:7])=[O:4]

Participants

4

Conditions

Temperature
115 °C

Procedure

To a mixture of isopropyl propiolate (350 g, 3.1 moles) in AcOH (1300 mL) was added NaI (930 g, 6.2 moles) at 25° C. The reaction mixture was heated to 115° C. and stirred for 1.5 hrs. The reaction mixture was cooled to 25 to 30° C. and quenched with water followed by extraction with MTBE. The organic layer was washed with saturated bicarbonate, bisulfite and brine solution. The organic layer was dried over sodium sulfate and concentrated under vacuum to give the product (Z)-isopropyl 3-iodoacrylate (626 g; 83.5%). Product was confirmed by 1H NMR.

Workup

  1. temperatureThe reaction mixture was cooled to 25 to 30° C.
  2. customquenched with water
  3. extractionfollowed by extraction with MTBE
  4. washThe organic layer was washed with saturated bicarbonate, bisulfite and brine solution
  5. dry with materialThe organic layer was dried over sodium sulfate
  6. concentrationconcentrated under vacuum

Sources & evidence

ORD record
ord-9e1076c336c6475db26479acde0e0baf
Source dataset
uspto-grants-2015_12
Patent number
US09206158B2

Reaction notes

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