HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Thienylmethyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-Thiophenemethanol | HCID 69467 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Thienylmethyl methanesulfonate | HCID 18973430 | — |
Reaction Steps
Methanesulphonyl chloride (6.2 mL, 0.0797 mol) is added dropwise to a solution of thiophene-2-methanol (7.0 g, 0.0613 mol) and triethyl amine (12.8 mL, 0.0920 mol) in dichloromethane (70 mL) at 0-5° C. The reaction mixture is allowed to stir at room temperature for 30 min. Demineralized water (25 mL) is added to the reaction mixture and the organic layer is separated. The aqueous layer is extracted with dichloromethane (1×25 mL). Combined organic layer is dried over anhydrous sodium sulfate. Removal of solvent under reduced pressure gives methanesulfonic acid thiophen-2-ylmethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09266867B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-152c9c9841ef4067891a61b3f95c33c8 |
| Source note | uspto-grants-2016_02 |