HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Methyl 4-(1-methanesulfonylamino-1-methylethyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Methyl 4-(1-amino-1-methylethyl)benzoate | HCID 57572309 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 4-(1-methanesulfonylamino-1-methylethyl)benzoate | HCID 71252533 | — |
Reaction Steps
Methyl 4-(1-amino-1-methylethyl)benzoate (200 mg) and triethylamine (0.30 mL) were dissolved in dichloromethane (10 mL), methanesulfonyl chloride (88 μL) was added under ice-cooling, and the mixture was stirred at the same temperature for 30 min and at room temperature for 2 hr. After completion of the reaction, the solvent was evaporated, 0.5N hydrochloric acid was added to the residue, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and the solvent was evaporated. The obtained residue was purified by column chromatography (hexane:ethyl acetate) to give the title compound (252 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08816079B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-8b6ba91e240f4d0d9a2833cb6411b75e |
| Source note | uspto-grants-2014_08 |