HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Benzyloxy) ethanol → 2-Benzyloxyethyl mesylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Benzyloxy) ethanol | HCID 12141 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2-Benzyloxyethyl mesylate | HCID 10857272 | — |
Reaction Steps
To a solution of 2-(benzyloxy)ethanol in 320 ml of dichloromethane, 35 ml of triethylamine and 19.5 ml of methanesulfonyl chloride were added under ice cooling, followed by stirring at room temperature for 2 hours. The reaction mixture was added with ice water and then extracted with dichloromethane. After the extract was washed with a saturated solution of sodium chloride, the extract was dried over magnesium sulfate and then filtered. The filtrate was concentrated under reduced pressure, whereby 49 g of 2-(benzyloxy)ethyl methanesulfonate were obtained (yield: stoichiometric).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05990139 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-26a9a54b5b09499695ec5eb3ca57f1ee |
| Source note | uspto-grants-1999_11 |