HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 5-Benzoylthio-2-methyl-2-(p-nitrobenzyloxycarbonyl)aminopentane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-p-Toluenesulfonyloxy-2-methyl-2-(p-nitrobenzyloxycarbonyl)aminopentane | HCID 20140775 | — |
| Reactant | HCID 178526132 | HCID 178526132 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Benzoylthio-2-methyl-2-(p-nitrobenzyloxycarbonyl)aminopentane | HCID 20140776 | — |
Reaction Steps
A mixture of thiobenzoic acid (890 mg) and sodium hydride (50%) (220 mg) in dimethylformamide (8 ml) was stirred for 10 minutes with ice-cooling. 5-p-Toluenesulfonyloxy-2-methyl-2-(p-nitrobenzyloxycarbonyl)aminopentane (1.64 g) in dimethylformamide (8 ml) was added thereto, followed by stirring for 25 minutes. The reaction mixture was diluted with ethyl acetate, washed with dilute hydrochloric acid and then water, dried over anhydrous sodium sulfate and evaporated to give an oily residue which was then purified by silica gel chromatography to give 5-benzoylthio-2-methyl-2-(p-nitrobenzyloxycarbonyl)aminopentane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04742052 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-5d36794649ab4b0999f1d0aed3840bbb |
| Source note | uspto-grants-1988_05 |