HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-cyanomethyl-N-methyl-2-phenoxybenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Acetonitrile, 2-(methylamino)-, hydrochloride (1:1) | HCID 117641 | — |
| Reactant | 2-Phenoxybenzoyl chloride | HCID 11075303 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-cyanomethyl-N-methyl-2-phenoxybenzamide | HCID 20333639 | — |
Reaction Steps
2.7 parts of methylaminoacetonitrile hydrochloride was added to a solution of 2 parts of sodium hydroxide in 25 parts of water at ~15°. When the addition was complete a solution of 5.8 parts of 2-phenoxybenzoyl chloride in 50 parts of methylene chloride was added dropwise. The mixture was stirred vigorously for 5 hrs. at ~20°. The methylene chloride layer was then separated, washed with water and dried over magnesium sulfate. Removal of the magnesium sulfate by filtration and concentration of the filtrate gave 4.6 parts of N-cyanomethyl-N-methyl-2-phenoxybenzamide as a viscous oil. NMR (CDCl3) 3δ(S,3H,CH3), 4.1δ,4.3δ (2S,2H,CH2), 7.05δ, (m,9H,Aromatic H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04208205 |
| Source dataset | uspto-grants-1980_06 |
| ORD ID | ord-8dd951a654b440ec948e08775ce8016d |
| Source note | uspto-grants-1980_06 |