HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → N-acetyl-2-(triphenylmethylthio)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzenemethanethiol, alpha,alpha-diphenyl- | HCID 77281 | — |
| Reactant | N-acetyl-2-chloroacetamide | HCID 2366697 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-acetyl-2-(triphenylmethylthio)acetamide | HCID 12837901 | — |
Reaction Steps
A mixture of 0.009 mole of triphenylmethyl mercaptan and 0.009 mole of triethylamine in 10 ml. of dimethylformamide is cooled to 0°-5° C. in an ice bath and 0.009 mole of N-acetyl-2-chloroacetamide added. The reaction mixture is stirred at ambient temperature for three hours and then poured into 100 ml. of benzene and 100 ml. of water. The organic layer is separated, washed well with water, dried over sodium sulfate and concentrated to dryness. The residue is crystallized under petroleum ether to give 2.2 g. of Nacetyl-2-(triphenylmethylthio) acetamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04329363 |
| Source dataset | uspto-grants-1982_05 |
| ORD ID | ord-fc25da623359446fa5544f1cfa018c21 |
| Source note | uspto-grants-1982_05 |