HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Furanethanol, tetrahydro-, 2-methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-(Oxolan-2-yl)ethan-1-ol | HCID 11989572 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Furanethanol, tetrahydro-, 2-methanesulfonate | HCID 57699687 | — |
Reaction Steps
To an ice cooled stirring solution of 2-(tetrahydrofuran-2-yl)ethanol (1.9 g) and triethylamine (4.4 ml) in dry dichloromethane (30 ml) was added dropwise over 5 min methanesulphonyl chloride (1.59 ml). The mixture was allowed to warm slowly to ambient temperature over 16 h then washed with saturated sodium hydrogen carbonate. The aqueous layer was further extracted with dichloromethane and the combined extracts washed with brine, dried by passing through a phase separation cartridge and stripped to give the title compound as a light brown oil, yield 3.1 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977344B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-91cbba8f2cc948cd933467443e275cda |
| Source note | uspto-grants-2011_07 |