Hydrochloric Acid → 2-Amino-3-fluorobenzoic acid

HRID 648743Notes

Reaction equation

HRID 648743 reaction equation
[F:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:10]=1[NH:9]C(=O)[C:7]2=[O:12].[OH-:13].[Na+].OO.Cl>O>[NH2:9][C:10]1[C:2]([F:1])=[CH:3][CH:4]=[CH:5][C:6]=1[C:7]([OH:12])=[O:13]

Participants

6

Conditions

Temperature
70 °C

Procedure

A mixture of 19.27 g of the product of Step B and 197 ml of 10N sodium hydroxide solution was heated to 70° C. with stirring and heating was ceased to add 36.5 ml of 30% hydrogen peroxide over 20 minutes during which the temperature rose to 80° C. and descended to 70° C. At the end of the addition, the mixture was heated to 80° C. and held there for 10 minutes and then was cooled during which a mass formed. The latter was added to 200 ml of water with stirring and the pH was adjusted to 1 by addition of concentrated hydrochloric acid at a temperature less than 20° C. The mixture was stirred for 90 minutes and was vacuum filtered. The product was empasted twice with iced water and dried under reduced pressure at 70° C. The product was crystallized from 100 ml of a 1-1 ethanol-water mixture and 3 ml of acetic acid. The mixture was iced for one hour and was vacuum filtered. The product was empasted with a 1-1 ethanol-water mixture and dried at 70° C. under reduced pressure to obtain 14.8 g of 2-amino-3-fluoro-benzoic acid melting at 188° C.

Workup

  1. temperatureheating
  2. customrose to 80° C.
  3. customdescended to 70° C
  4. additionAt the end of the addition
  5. temperaturethe mixture was heated to 80° C.
  6. temperaturewas cooled during which a mass
  7. customformed
  8. stirringwith stirring
  9. stirringThe mixture was stirred for 90 minutes
  10. filtrationfiltered
  11. customdried under reduced pressure at 70° C
  12. customThe product was crystallized from 100 ml of a 1-1 ethanol-water mixture and 3 ml of acetic acid
  13. waitThe mixture was iced for one hour
  14. filtrationfiltered
  15. customdried at 70° C. under reduced pressure

Sources & evidence

ORD record
ord-38f156c34e6040289ff3047bd5f8975b
Source dataset
uspto-grants-1988_04
Patent number
US04736033

Reaction notes

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