HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4,4,4-Trifluorobutyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4,4,4-Trifluorobutan-1-ol | HCID 136307 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4,4,4-Trifluorobutyl methanesulfonate | HCID 22725681 | 988% |
Reaction Steps
A stirred solution of 4,4,4-trifluorobutanol (35 g; 0.027 mol) and triethylamine (28.3 g; 0.280 mol) in 200 ml of dichloromethane was treated dropwise at 0° C. with a solution of methanesulphonyl chloride (32.1 g; 0.280 mol) in 100 ml of dichloromethane. After the end of the addition, the mixture was stirred for a further 30 min, then poured onto ice and the phases were subsequently separated. The organic phase was dried over magnesium sulphate and concentrated under reduced pressure. 55 g of crude 4,4,4-trifluorobutyl methanesulphonate were obtained as an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06262112B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-d8f8b65e30d24eddbcc696f323a79f82 |
| Source note | uspto-grants-2001_07 |