HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 7-(Tetrahydropyran-2-yloxy)heptyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1-Heptanol, 7-[(tetrahydro-2H-pyran-2-yl)oxy]- | HCID 10398424 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 7-(Tetrahydropyran-2-yloxy)heptyl methanesulfonate | HCID 15097251 | — |
Reaction Steps
A solution of 2.32 ml of methanesulfonyl chloride dissolved in 10 ml of benzene was added dropwise, whilst ice-cooling, to a solution of 4.32 g of 7-(tetrahydropyran-2-yloxy)-1-heptanol and 5.56 ml of triethylamine dissolved in 80 ml of benzene. The mixture was stirred at room temperature for 1 hour, after which it was washed with water, dried over anhydrous magnesium sulfate and concentrated by evaporation under reduced pressure, to give 5.86 g of 7-(tetrahydropyran-2-yloxy)heptyl methanesulfonate, as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04891363 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-965ab1cac64e421082060df57d0383c6 |
| Source note | uspto-grants-1990_01 |