Water → Ethyl-2-(10H-phenoxazin-10-yl)acetate

HRID 2219778Notes

Reaction equation

HRID 2219778 reaction equation
[CH:1]1[C:14]2[NH:13][C:12]3[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=3)[O:6][C:5]=2[CH:4]=[CH:3][CH:2]=1.[H-].[Na+].Br[CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20].O>CN(C)C=O>[CH2:22]([O:21][C:19](=[O:20])[CH2:18][N:13]1[C:14]2[CH:1]=[CH:2][CH:3]=[CH:4][C:5]=2[O:6][C:7]2[C:12]1=[CH:11][CH:10]=[CH:9][CH:8]=2)[CH3:23]

Participants

6

Conditions

Temperature
80 °C

Procedure

A solution of phenoxazine (10 g, 54.6 mmol) in dry dimethyl formamide (15 ml) was added slowly to a stirred ice cooled suspension of sodium hydride (60% dispersion in oil) (2.88 g, 60.1 mmol) in dimethyl formamide (10 ml), under an atmosphere of nitrogen. The mixture was stirred at 80° C. for 2 h and cooled to 0° C. and ethyl bromoacetate (12.78 g, 76.50 mmol) was added dropwise and stirring was continued for 12 h at 25° C. (TLC monitored). Water (50 ml) was added and the aqueous phase extracted with ethyl acetate (2×75 ml). The combined organic phases were washed with water (50 ml), brine (5 ml), dried (Na2SO4), filtered and the solvent was evaporated under reduced pressure. The residue was chromatographed over silica gel (100-200 mesh) using a mixture of benzene and petroleum ether (1:1) to afford the title compound (5.7 g, 39%) as a pale bluish green solid. mp: 96-97° C.

Workup

  1. temperaturecooled
  2. temperaturecooled to 0° C.
  3. stirringstirring
  4. waitwas continued for 12 h at 25° C.
  5. extractionthe aqueous phase extracted with ethyl acetate (2×75 ml)
  6. washThe combined organic phases were washed with water (50 ml), brine (5 ml)
  7. dry with materialdried (Na2SO4)
  8. filtrationfiltered
  9. customthe solvent was evaporated under reduced pressure
  10. customThe residue was chromatographed over silica gel (100-200 mesh)
  11. additiona mixture of benzene and petroleum ether (1:1)

Sources & evidence

ORD record
ord-97fb3645204649c4af728928df5db143
Source dataset
uspto-grants-2008_08
Patent number
US07414128B2

Reaction notes

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