Sodium Methoxide → METHYL 2-METHYL-4-OXOCYCLOHEX-2-ENECARBOXYLATE

HRID 2283485Notes

Reaction equation

HRID 2283485 reaction equation
C[O-].[Na+].[CH3:4][C:5]1[CH:10]([C:11]([O:13][CH3:14])=[O:12])[CH2:9][CH2:8][C:7](=[O:15])[C:6]=1C(OC)=O>CO>[CH3:4][C:5]1[CH:10]([C:11]([O:13][CH3:14])=[O:12])[CH2:9][CH2:8][C:7](=[O:15])[CH:6]=1

Participants

4

Conditions

Temperature
80 °C

Procedure

To a solution of sodium methanolate (90 g, 1.67 mol) in methanol (300 mL) was added dimethyl 2-methyl-6-oxocyclohex-1-ene-1,3-dicarboxylate (150 g, 663.04 mmol) in methanol (150 mL) dropwise with stirring over 30 minutes. The resulting solution was heated to 80° C. for 30 minutes, and the mixture was concentrated in vacuo. The reaction mixture was diluted with H2O/ice (120 mL); then diluted furtherwith acetic acid (130 mL). The resulting solution was extracted with Et2O (3×), and the organic layers were combined and dried over Na2SO4, filtered, and concentrated in vacuo. The final product was purified by distillation under reduced pressure (5 mm Hg), and the fraction was collected at 110˜120° C. Methyl 2-methyl-4-oxocyclohex-2-enecarboxylate was obtained as a yellow oil. MS ESI calcd. for C9H13O3 [M+H]+ 169. found 169.

Workup

  1. concentrationthe mixture was concentrated in vacuo
  2. additionThe reaction mixture was diluted with H2O/ice (120 mL)
  3. additionthen diluted furtherwith acetic acid (130 mL)
  4. extractionThe resulting solution was extracted with Et2O (3×)
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. distillationThe final product was purified by distillation under reduced pressure (5 mm Hg)
  9. customthe fraction was collected at 110˜120° C

Sources & evidence

ORD record
ord-17b85e2f859949b6a0e754436e6a92e5
Source dataset
uspto-grants-2015_09
Patent number
US09145391B2

Reaction notes

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