Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 2-(4-oxo-3,4-dihydrophthalazin-1-yl)acetate | HCID 348622 | — |
| Reactant | HCID 54421939 | HCID 54421939 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 60204236 | HCID 60204236 | — |
Reaction Steps
64.8 g (1.62 mol) of a 60% suspension of sodium hydride in oil are added portionwise under a nitrogen atmosphere to a solution of 341.9 g (1.472 mol) of ethyl 3,4-dihydro-4-oxo-1-phthalazineacetate (prepared according to the process described in Patent EP 2895) in 5 l of anhydrous DMF, the temperature being maintained between 25° and 30° C. The addition lasts approximately one hour. The mixture is then heated for 30 minutes at 60° C. The mixture is cooled to room temperature and a mixture of 421.6 g (1.76 mol) of 1-(3-chloro-1-propenyl) -2-fluoro-3-(trifluoromethyl) benzene (prepared according to Example D1) and 98 ml of anhydrous DMF is added over 30 min. The temperature rises to 38° to 40° C. The mixture is then heated for 3 hours at 60° C. and is then allowed to return to room temperature overnight. The mixture is poured into 7 l of water and extracted with 2 times 4 l of ethyl acetate. Washing is carried out with water, the organic phase is dried over Na2SO4, filtered and evaporated under vacuum and the solid obtained is recrystallized from a hexane/ethyl acetate (4/1 ) mixture. Weight obtained: 474.7 g (Yd.=74%) M.p.=104°-106° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05489592 |
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| Source dataset | uspto-grants-1996_02 |
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| ORD ID | ord-68a17cdb12124b9a9efd0ad9cf2dec77 |
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| Source note | uspto-grants-1996_02 |
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