HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(Tetrahydro-3-furanyl)ethyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-(Oxolan-3-yl)ethan-1-ol | HCID 11126225 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Tetrahydro-3-furanyl)ethyl methanesulfonate | HCID 57699822 | — |
Reaction Steps
2-(Tetrahydro-3-furanyl)ethanol (230 mg) was dissolved in dry DCM (5 mL) and triethylamine (0.552 mL) was added. The stirred solution was cooled (ice bath) under nitrogen and methanesulphonyl chloride (0.199 mL) was added dropwise over 5 mins. The mixture was allowed to warm slowly to room temperature as the ice bath melted and was left for 16 h. The mixture was shaken with saturated sodium bicarbonate solution and the aqueous layer was extracted with DCM (×2). The combined organics were washed with brine, dried using a hydrophobic frit and evaporated to give the title compound (364 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977344B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-6d6052d02976479ead74394d279bfd66 |
| Source note | uspto-grants-2011_07 |