HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → N-methyl-2-(4-chlorophenyl)-2-cyano-5-phenylthiovaleroamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Methyl isothiocyanate | HCID 11167 | — |
| Reactant | 2-(4-Chlorophenyl)-5-phenylvaleronitrile | HCID 14147722 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-methyl-2-(4-chlorophenyl)-2-cyano-5-phenylthiovaleroamide | HCID 19794677 | 52.6% |
Reaction Steps
To a tetrahydrofuran solution containing 1.78 g (6.6 mmole) of 2-(4-chlorophenyl)-5-phenylvaleronitrile was added a tetrahydrofuran solution containing 0.77 g (6.9 mmole) of potassium tert-butoxide at 0° C. After stirring for 30 minutes, a tetrahydrofuran solution containing 0.5 g (6.8 mmol) of methyl isothiocyanate was added to the mixture and the mixture was stirred at room temperature for 2 hours. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate, dried and condensed under reduced pressure, and then purified by silica gel chromatography to obtain 1.19 g (yield: 52.4 %) of N-methyl-2-(4-chlorophenyl)-2-cyano-5-phenylthiovaleroamide as a crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05246958 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-9eff2be66d41411fafc7473e558a11ff |
| Source note | uspto-grants-1993_09 |