HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(Cyanomethyl) 2-acetoxy 4-acetamino 5-chlorobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Aminoacetonitrile hydrochloride | HCID 11491918 | — |
| Reactant | 2-acetoxy 4-acetamino 5-chlorobenzoyl Chloride | HCID 20163776 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-(Cyanomethyl) 2-acetoxy 4-acetamino 5-chlorobenzamide | HCID 54344079 | — |
Reaction Conditions
| Temperature | 5 °C |
|---|
Reaction Steps
104 g of triethylamine and 890 cc of chloroform were introduced into a 3 liter balloon flask provided with a sealed agitator, a reflux condenser and a thermometer. The solution obtained was cooled to 5° C. 51 g of amino acetonitrile hydrochloride was then gradually added, with the temperature being maintained at between 5° and 10° C. Thereafter over a period of 30 minutes and at a temperature of between 0° and 5° C., 143 g of 2-acetoxy 4-acetamino 5-chlorobenzoyl chloride in finely divided form was added. A dark-coloured solution resulted, which was agitated, first, for a period of 2 hours at 10° C. and, thereafter, for 2 hours at ambient temperature.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04703055 |
| Source dataset | uspto-grants-1987_10 |
| ORD ID | ord-d48e83ed5b444f4c9689eca66cfc0423 |
| Source note | uspto-grants-1987_10 |