HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 1,2-Ethanediol, 1,2-dimethanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Toluene methylene chloride | HCID 21877217 | — |
| Product | 1,2-Ethanediol, 1,2-dimethanesulfonate | HCID 20796 | — |
Reaction Steps
Potassium carbonate (6.7 g, 48.5 mmol) and diisopropylethylamine (0.3 g, 2.3 mmol) were suspended in dichloromethane-toluene (1/1, 10 mL), and ethylene glycol (1.5 g, 23.3 mmol) and methanesulfonyl chloride (5.5 g, 48.0 mmol) were dropped at the same time in an ice bath. A reaction was effected at room temperature for 3 hours and, thereafter, the reaction was terminated by addition to ice water. An organic layer separated through liquid separation was concentrated, so as to obtain the desired product, 1,2-bis(methanesulfonyloxy)ethane, at a yield of 36% (1.8 g, 8.4 mmol). The measurement result of 1H NMR is as described below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08716513B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-d8d69f21d68e4417a51945fb50233f1c |
| Source note | uspto-grants-2014_05 |