2-Aminophenol → 2H-1,4-benzoxazin-3(4H)-one

HRID 1109465Notes

Reaction equation

HRID 1109465 reaction equation
Cl[CH2:2][C:3](Cl)=[O:4].[NH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[OH:13].[Cl-].C(C[NH3+])C1C=CC=CC=1.C(=O)(O)[O-].[Na+]>C(Cl)(Cl)Cl>[O:4]=[C:3]1[NH:6][C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=2[O:13][CH2:2]1

Participants

6

Procedure

A solution of chloroacetyl chloride (31.2 g) in chloroform (100 ml) was added dropwise to a mixture of 2-aminophenol (25 g), benzylmethylammonium chloride (52.4 g), sodium bicarbonate (77 g) and chloroform (500 ml) which was cooled in an ice-bath. The mixture was stirred for 1 hour and allowed to warm to ambient temperature. The mixture was heated to 55° C. for 5 hours and then stirred at ambient temperature for 16 hours. The mixture was evaporated and the residue was partitioned between ethyl acetate and an aqueous solution of potassium carbonate. The organic phase was washed with dilute aqueous hydrochloric acid and with water, dried (MgSO4) and evaporated. The residue was washed with a mixture of hexane and diethyl ether to leave 3-oxo-2,3-dihydro-4H-1,4-benzoxazine (11 g, 32%) m.p. 172°-173° C.

Workup

  1. temperaturewas cooled in an ice-bath
  2. temperatureThe mixture was heated to 55° C. for 5 hours
  3. stirringstirred at ambient temperature for 16 hours
  4. customThe mixture was evaporated
  5. customthe residue was partitioned between ethyl acetate
  6. washThe organic phase was washed with dilute aqueous hydrochloric acid and with water
  7. dry with materialdried (MgSO4)
  8. customevaporated
  9. washThe residue was washed with a mixture of hexane and diethyl ether

Sources & evidence

ORD record
ord-42bc1ba8d2c94efda2a04a8390ceb103
Source dataset
uspto-grants-1994_06
Patent number
US05321025

Reaction notes

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