HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Methanesulphonic acid 2-(6-methoxyindan-1-yl)ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-(6-Methoxyindan-1-yl)ethanol | HCID 10997857 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methanesulphonic acid 2-(6-methoxyindan-1-yl)ethyl ester | HCID 53897303 | — |
Reaction Steps
5.0 g (26.0 mmol) of crude 2-(6-methoxyindan-1-yl)ethanol are dissolved in 50 ml of dichloromethane and, while cooling with ice, 3.6 g (31 mmol) of methanesulphonic acid chloride and 3.1 g (31 mmol) of triethylamine are added dropwise. The mixture is stirred at room temperature for 3 hours, the triethylammonium chloride which has precipitated is filtered off and the filtrate is extracted by shaking with ice-water. The organic phases are washed with saturated sodium chloride solution, dried over magnesium sulphate and concentrated by evaporation at 40° under reduced pressure. Methanesulphonic acid 2-(6-methoxyindan-1-yl)ethyl ester is obtained which can be used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04833169 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-5b94a7c5ec374035b1be7a9f5adcf065 |
| Source note | uspto-grants-1989_05 |