Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | HCID 8713889 | HCID 8713889 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 68774932 | HCID 68774932 | — |
Reaction Steps
To a solution of N-(3-bromophenyl)-2,6-difluorobenzamide in 200 mL of DMF at room temperature and under nitrogen atmosphere, NaH 60% in oil dispersion (104.7 mmol) is slowly added and the reaction mixture is stirred for 30 minutes. Tert-butylbromoacetate (104.7 mmol) is added and the reaction stirred at room temperature. After 12 hours the reaction is complete by TLC (hexanes:ethyl acetate=8:2) and analytical LCMS (20 to 100% CH3CN). Ethyl acetate and water are added to the reaction mixture and the phases are separated. The organic phase is dried on sodium sulfate, filtered and the solvent is evaporated. The crude is purified by automated column chromatography (gradient of hexanes and ethyl acetate) to give tert-butyl 2-(N-(3-bromophenyl)-2,6-difluorobenzamido)acetate: 1H NMR (400 MHz, CDCl3) δ 7.36 (bs, 1H), 7.20 (m, 1H), 7.07 (m, 2H), 6.96 (t, J=8 Hz, 1H), 6.62 (td, J=8 Hz, J2=1.2 Hz), 4.32 (s, 2H), 1.39 (s, 9H); MS: (ES+) 448.0 (M+23)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07846949B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-ccae709e33004cea8f7c87c1bb7ef06d |
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| Source note | uspto-grants-2010_12 |
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