Toluene → Tetrahydrofuran toluene

HRID 892229Notes

Reaction equation

HRID 892229 reaction equation
[Na][CH:2]([C:6]([O-])=O)[C:3]([O-])=[O:4].[C:9]([O-])(=O)CC([O-])=O.[H-].[Na+].[C:18]1([CH3:24])[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>C1COCC1.CCOCC.O>[C:18]1([CH3:24])[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1.[CH2:6]1[CH2:9][O:4][CH2:3][CH2:2]1

Participants

8

Procedure

A solution of Mo(CO)3(EtCN)3 and ligand in toluene was heated at 60–70° C. for 1 h. A solution of sodiomalonate (prepared by adding the malonate to sodium hydride (60% dispersion in oil)) and the substrate in THF was added dropwise via syringe at 60° C. and the mixture was heated at 80–90° C. for the time indicated. The reaction mixture was diluted with ether (5 mL) and water (5 mL) was added. The layers were separated and the aqueous layer was extracted with ether (3×10 mL). The combined organic layers were washed with brine (10 mL), dried over magnesium sulfate and the solvent removed in vacuo. Flash chromatography (with the solvent system indicated) afforded the product as a mixture of the two regioisomers.

Workup

  1. additionwas added dropwise via syringe at 60° C.
  2. temperaturethe mixture was heated at 80–90° C. for the time
  3. additionwas added
  4. customThe layers were separated
  5. extractionthe aqueous layer was extracted with ether (3×10 mL)
  6. washThe combined organic layers were washed with brine (10 mL)
  7. dry with materialdried over magnesium sulfate
  8. customthe solvent removed in vacuo
  9. customafforded the product
  10. additionas a mixture of the two regioisomers

Sources & evidence

ORD record
ord-293d6cb0692f409e8c050742b9cf5069
Source dataset
uspto-grants-2006_02
Patent number
US07005521B1

Reaction notes

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