Dimethyl Carbonate → HCID 178499032, compound

HRID 593303Notes

Reaction equation

HRID 593303 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[C:7](=[O:11])[CH2:6][CH2:5]2.[H-].[Na+:13].[C:14](=O)([O:17][CH3:18])[O:15]C.[OH-].[Na+]>C1COCC1.C(OCC)C>[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[C:7](=[O:11])[C:6]([Na:13])([C:14]([O:17][CH3:18])=[O:15])[CH2:5]2

Participants

7

Procedure

5-Bromo indanone (8 g, 37.9 mmol) was added to an ice cold solution of sodium hydride (2.72 g, 113.3 mmol) in THF (100 mL) and stirred at room temperature for 30 min. Dimethyl carbonate (17.25 g, 189.56 mmol) was then added and mixture was refluxed for 16 h. Reaction mixture was cooled to room temperature and poured into ice water. pH of solution was made basic using saturated aqueous solution of NaOH solution and extracted with twice with ethyl acetate and concentrated under vacuum. Residue obtained was dissolved in diethyl ether and cooled to 0° C. A solution of saturated aqueous solution of NaOH was added (10 mL) while stirring. Resulting sodium salt was collected by filtration and dried under vacuum to afford crude title compound (7 g) as solid. 1H NMR (400 MHz, DMSO-d6): δ 7.52 (s, 1H), 7.40 (m, 1H), 7.34 (m, 1H), 3.52 (s, 3H), 3.3 (s, 2H).

Workup

  1. temperaturemixture was refluxed for 16 h
  2. customReaction mixture
  3. temperaturewas cooled to room temperature
  4. extractionextracted with twice with ethyl acetate
  5. concentrationconcentrated under vacuum
  6. customResidue obtained
  7. temperaturecooled to 0° C
  8. stirringwhile stirring
  9. filtrationResulting sodium salt was collected by filtration
  10. customdried under vacuum

Sources & evidence

ORD record
ord-df8e9bbc33094420a45a80617ba7b2f7
Source dataset
uspto-grants-2016_01
Patent number
US09242929B2

Reaction notes

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