HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → 2-[(2-bromophenyl)-hydrazono]-N-methyl-2-cyanoacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | [(2-Bromophenyl)-hydrazono]-cyanoacetic acid ethyl ester | HCID 4084583 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[(2-bromophenyl)-hydrazono]-N-methyl-2-cyanoacetamide | HCID 86613099 | — |
Reaction Steps
[(2-Bromophenyl)-hydrazono]-cyanoacetic acid ethyl ester (15.28 g, 51.60 mmol) was dissolved in 40% methylamine in water (67.5 mL) and stirred at room temperature overnight. The reaction mixture was concentrated to dryness, slurried in diethyl ether, and filtered. After drying under high vacuum at 40° C., the title compound was obtained as a yellow solid (11.16 g, 77%). 1H NMR (300.132 MHz, CDCl3) δ 7.68 (dd, J=8.2, 1.4 Hz, 1H), 7.54 (dd, J=8.1, 1.3 Hz, 1H), 7.35 (t, J=7.9 Hz, 1H), 7.01 (td, J=7.7, 1.5 Hz, 1H), 6.29 (s, 1H), 2.98 (d, J=4.9 Hz, 3H). MS APCI, m/z=281/283 (M+H). HPLC 4.08 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07465795B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-a82ec8a6d9694b508ca413e223cdc74f |
| Source note | uspto-grants-2008_12 |