HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-Cyclopropyl-3-(2-nitrophenyl)-propyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1-Cyclopropyl-3-(2-nitrophenyl)-propan-1-ol | HCID 20389978 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Cyclopropyl-3-(2-nitrophenyl)-propyl methanesulfonate | HCID 86621242 | — |
Reaction Steps
A mixture of 0.5 g of 1-cyclopropyl-3-(2-nitrophenyl)-propan-1-ol (2.26 mmol), 0.26 g of triethylamine (2.6 mmol) and 12 ml of dichloromethane is cooled to a temperature of 5° C. and 0.28 g of methanesulfonic acid chloride, dissolved in 3 ml of dichloromethane, is added dropwise. The resulting mixture is stirred for 16 hours at ambient temperature. The organic phase is washed with ice-water and dried over sodium sulfate and concentrated by evaporation. 1-Cyclopropyl-3-(2-nitrophenyl)-propyl methanesulfonate is obtained in the form of a crude product, which is used directly in the cyclisation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07514584B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-4462d1eaab1543dab56f2fa0764df602 |
| Source note | uspto-grants-2009_04 |