Methyl iodide → 6-Methoxy-2,3-dihydrobenzo[b][1,4]dioxine

HRID 594285Notes

Reaction equation

HRID 594285 reaction equation
[O:1]1[CH2:6][CH2:5][O:4][C:3]2[CH:7]=[C:8]([OH:11])[CH:9]=[CH:10][C:2]1=2.[C:12]([O-])([O-])=O.[K+].[K+].IC>CC(C)=O>[CH3:12][O:11][C:8]1[CH:9]=[CH:10][C:2]2[O:1][CH2:6][CH2:5][O:4][C:3]=2[CH:7]=1

Participants

5

Procedure

A mixture of 2,3-dihydrobenzo[b][1,4]dioxin-6-ol (2.600 g; 17.10 mmol), and K2CO3 (2.598 g; 18.80 mmol) in anh. acetone (40 ml) was stirred at rt, under nitrogen, for 1 h. Iodomethane (13.340 g; 94.00 mmol) was then added, and the resulting mixture was heated at reflux, under nitrogen, for 2 h. After cooling to rt, the reaction mixture was filtered over a pad of celite, and the filtrate was concentrated to dryness under reduced pressure. Et2O and water were added, and the organic layer was further washed with brine, dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure affording 6-methoxy-2,3-dihydrobenzo[b][1,4]dioxine as a yellow oil. LC-MS (conditions A): tR=0.65 min.; [M+H]+: 167.11 g/mol.

Workup

  1. temperaturethe resulting mixture was heated
  2. temperatureat reflux, under nitrogen, for 2 h
  3. temperatureAfter cooling to rt
  4. filtrationthe reaction mixture was filtered over a pad of celite
  5. concentrationthe filtrate was concentrated to dryness under reduced pressure
  6. additionEt2O and water were added
  7. washthe organic layer was further washed with brine
  8. dry with materialdried over anh. MgSO4
  9. filtrationfiltered
  10. concentrationconcentrated to dryness under reduced pressure

Sources & evidence

ORD record
ord-af550a2c5d5247f1a9802c8b39d259ef
Source dataset
uspto-grants-2016_01
Patent number
US09242970B2

Reaction notes

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