HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Oxan-4-ylmethyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (Oxan-4-yl)methanol | HCID 2773573 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Oxan-4-ylmethyl methanesulfonate | HCID 15166436 | — |
Reaction Steps
To tetrahydro-2H-pyran-4-ylmethanol (6.2 g) in dry dichloromethane (226.3 ml) at 0° C. and under nitrogen, was added triethylamine (18.1 ml), followed by mesyl chloride (5.4 ml). The reaction was allowed to warm to room temperature and left at this temperature overnight. The reaction mixture was washed with saturated aqueous sodium bicarbonate (200 ml). The organic layer was separated, passed through a hydrophobic frit to dry and concentrated in vacuo to yield a light brown lumpy solid (10.17 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977344B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-1c79bcc0a48f4c788f711db359048136 |
| Source note | uspto-grants-2011_07 |