Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Reactant | (4-Oxo-3,4-dihydrophthalazin-1-yl)acetic acid | HCID 348621 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 20495830 | HCID 20495830 | 16.4% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04393062 |
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| Source dataset | uspto-grants-1983_07 |
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| ORD ID | ord-28b9733dee3946dba017115586e83ca7 |
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| Source note | uspto-grants-1983_07 |
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