Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 3-Cyanobenzoyl chloride | HCID 308483 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Cyano-N-methylbenzamide | HCID 22049696 | — |
Reaction Steps
A mixture of 40% aqueous methylamine solution (20 ml) and THF (30 ml) was cooled to 5° C., and 3-cyanobenzoyl chloride (1.89 g) was slowly added. The mixture was stirred for one hr. The reaction mixture was extracted with ethyl acetate, and the organic layer was dried and concentrated. The residue was recrystallized from ethyl acetate to give the title compound (1.14 g) as colorless needle crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07067537B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-f0ba064e98704e17b2865c55a6045f08 |
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| Source note | uspto-grants-2006_06 |
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