HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-(2-(Tetrahydropyran-2-yloxy)ethyl)phenethyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-(2-(Tetrahydropyran-2-yloxy)ethyl)phenethyl alcohol | HCID 54236907 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(2-(Tetrahydropyran-2-yloxy)ethyl)phenethyl methanesulfonate | HCID 22407594 | 99.9% |
Reaction Steps
Triethylamine (3.22 g, 31.82 mmol) was added to a solution of 4-(2-(tetrahydropyran-2-yloxy)ethyl)phenethyl alcohol (4.00 g, 15.97 mmol) in methylene chloride (40 ml). The mixture was stirred under ice-cooling, and methanesulfonyl chloride (2.19 g, 19.11 mmol) was added dropwise to the mixture. After the addition, the resulting mixture was stirred under ice-cooling for 10 minutes. Then, water (40 ml) was added. The mixture was extracted with methylene chloride and dried over magnesium sulfate. Evaporation of the solvent gave the desired 4-(2-(tetrahydropyran-2-yloxy)ethyl)phenethyl methanesulfonate (5.24 g, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05519139 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-5981e944546a49d4847d6ab1f211e83c |
| Source note | uspto-grants-1996_05 |