Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 21285511 | HCID 21285511 | — |
| Reactant | HCID 178430880 | HCID 178430880 | — |
| Product | HCID 21285537 | HCID 21285537 | — |
Reaction Steps
A mixture of 2,4-dimethylimidazole (6.25 g), ethyl N-trifluoroacetyl-N-(5-fluoro-2-nitrobenzyl)glycinate (22.0 g) and sodium carbonate (6.62 g) was stirred and heated at 130° for 2 hours. Volatile material was removed from the cooled mixture in vacuo and the residue was partitioned between ethyl acetate (200 cm3) and water (100 cm3). The organic phase was washed with water (2×25 cm3), dried (MgSO4), and evaporated in vacuo to give an oil which was chromatographed on silica (Merck "MK 60.9385" [Trade Mark]) eluting with ethyl acetate:methanol, 1:19. Combination and evaporation of the appropriate fractions gave an oil which crystallised on trituration with ether to afford the title compound, m.p. 172.5°-176° (3.1 g). Analysis %: Found: C,50.7; H,4.8; N,12.7; Calculated for C18H19F3N4O5 : C,50.5; H,4.5; N,13.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04783467 |
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| Source dataset | uspto-grants-1988_11 |
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| ORD ID | ord-e18878f8af0a432e910575e99a78a2df |
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| Source note | uspto-grants-1988_11 |
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