HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetyl chloride → N-(Cyanomethyl)-2-phenylethanimidic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Aminoacetonitrile hydrochloride | HCID 11491918 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-(Cyanomethyl)-2-phenylethanimidic acid | HCID 231599 | — |
Reaction Steps
To aminoacetonitrile hydrochloride and 40 g (0.4 moles) triethylamine in 300 ml chloroform which was then cooled in an ice bath, the acid chloride from step (a) in 50 ml chloroform was dropped in over 60 minutes. The reaction mixture was washed three times with 200 ml water, dried over magnesium sulfate and stripped to give an oil. The oil was rubbed with 50 ml hexane and immediately solidified to give 30.4 g of beige solids, melting point 87° C. to 91° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04785019 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-b7cfd4dd3d6b4db4ab0f209974ddf004 |
| Source note | uspto-grants-1988_11 |