Sodium Hydroxide → HCID 20495830, compound

HRID 1074548Notes

Reaction equation

HRID 1074548 reaction equation
[O:1]=[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([CH2:12][C:13]([OH:15])=[O:14])=[N:4][NH:3]1.[OH-].[Na+].[Br:18][C:19]1[CH:26]=[CH:25][C:22]([CH2:23]Br)=[CH:21][CH:20]=1>CO>[Br:18][C:19]1[CH:26]=[CH:25][C:22]([CH2:23][N:3]2[N:4]=[C:5]([CH2:12][C:13]([OH:15])=[O:14])[C:6]3[C:11](=[CH:10][CH:9]=[CH:8][CH:7]=3)[C:2]2=[O:1])=[CH:21][CH:20]=1

Participants

5

Procedure

1,2-Dihydro-1-oxophthalazin-4-ylacetic acid (2.0 g.) was added to a solution of sodium hydroxide (0.9 g.) in methanol (50 ml.). A clear solution was obtained on slight warming, which was treated with 4-bromobenzyl bromide (2.6 g.). The mixture was then heated under reflux for 3 hours and then evaporated. The residue was treated with water (60 ml.) and the solution obtained was extracted with ether (3×60 ml.). The aqueous phase was then acidified to pH 2 with concentrated hydrochloric acid and the acid mixture extracted with ethyl acetate (150 ml.). The extracts were washed with water (50 ml.), dried (MgSO4) and evaporated. The solid obtained was recrystallised from a 1:4 v/v mixture of ethyl acetate and petrol (60-80) to give 2-(4-bromobenzyl)-1,2-dihydro-1-oxophthalazin-4-ylacetic acid (0.6 g.), m.p. 179°-181° C.

Workup

  1. customA clear solution was obtained on slight warming, which
  2. temperatureThe mixture was then heated
  3. temperatureunder reflux for 3 hours
  4. customevaporated
  5. additionThe residue was treated with water (60 ml.)
  6. customthe solution obtained
  7. extractionwas extracted with ether (3×60 ml.)
  8. extractionthe acid mixture extracted with ethyl acetate (150 ml.)
  9. washThe extracts were washed with water (50 ml.)
  10. dry with materialdried (MgSO4)
  11. customevaporated
  12. customThe solid obtained
  13. customwas recrystallised from a 1:4 v/v mixture of ethyl acetate and petrol (60-80)

Sources & evidence

ORD record
ord-28b9733dee3946dba017115586e83ca7
Source dataset
uspto-grants-1983_07
Patent number
US04393062

Reaction notes

Loading…