Ethyl 2-(oxetan-3-ylidene)propanoate → Ethyl 2-(oxetan-3-yl)propanoate

HRID 2202570Notes

Reaction equation

HRID 2202570 reaction equation
[O:1]1[CH2:4][C:3](=[C:5]([CH3:11])[C:6]([O:8][CH2:9][CH3:10])=[O:7])[CH2:2]1>CCO.[Pd]>[O:1]1[CH2:2][CH:3]([CH:5]([CH3:11])[C:6]([O:8][CH2:9][CH3:10])=[O:7])[CH2:4]1

Participants

4

Reactant 1

HCID 86698951Ethyl 2-(oxetan-3-ylidene)propanoate

Product 1

HCID 86698952Ethyl 2-(oxetan-3-yl)propanoate

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 702EthanolSolvent

Procedure

To a solution of (i) (151 mg, 0.97 mmol) in EtOH (54 mL) was added 10% Pd/C (50 mg, 0.05 mmol). The reaction was degassed and purged with hydrogen at balloon pressure (×3) then stirred under hydrogen at RT for 16 h. The reaction mixture was filtered and the residue washed with acetonitrile (10 mL). The combined organics were concentrated in vacuo and the residue, (ii) (148 mg), was used without further purification.

Workup

  1. customThe reaction was degassed
  2. custompurged with hydrogen at balloon pressure (×3)
  3. filtrationThe reaction mixture was filtered
  4. washthe residue washed with acetonitrile (10 mL)
  5. concentrationThe combined organics were concentrated in vacuo
  6. customthe residue, (ii) (148 mg), was used without further purification

Sources & evidence

ORD record
ord-3c970b877a9b4bc5841d602b2bc04e07
Source dataset
uspto-grants-2016_06
Patent number
US09365554B2

Reaction notes

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