Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methylamine | HCID 6329 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | Propylphosphonic anhydride | HCID 111923 | — |
| Edukt | 5-Bromo-2-methylbenzoic acid | HCID 346004 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 5-bromo-N,2-dimethylbenzamide | HCID 23156913 | 94,6% |
Reaktionsschritte
To a solution of 5-bromo-2-methylbenzoic acid (2.325 mmol, 0.5 g) in dichloromethane (25 mL) under nitrogen was added N,N-diisopropylethylamine (0.75 g, 5.8 mmol). Reaction then cooled in an ice bath to 2° C. and the yellow solution treated with 2M methylamine in tetrahydrofuran (3.49 mL, 6.98 mmol) over 5 minutes, followed by 1-propanephosphonic acid cyclic anhydride as a 50% wt solution in ethyl acetate (2.08 mL, 3.49 mmol) added dropwise. The ice bath was then removed and stirring continued overnight. The mixture was purified on silica (15 g column on Isolera 4) eluting with 0-5% methanol in dichloromethane to afford 5-Bromo-N,2-dimethylbenzamide (0.5 g, 2.2 mmol).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08841289B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-615c3d162ed9479c98fc676cd4fdb006 |
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| Quellennotiz | uspto-grants-2014_09 |
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