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 | 38% |
Reaction Steps
To a 0° C. mixture of 2-thiophenemethanol (2.80 g, 24.5 mmol) and triethylamine (5.10 mL, 36.8 mmol) in CH2Cl2 (25 mL) was added methanesulfonyl chloride (2.09 mL, 27.0 mmol) and the reaction mixture was stirred for 2 hours. The reaction mixture was poured into H2O and the layers were separated. The organic phase was washed with cold 1N HCl (3×), saturated aqueous NaHCO3, and brine, dried over MgSO4, filtered. and concentrated in vacuo. 2-thienylmethyl methanesulfonate (1.78 g, 38%) was obtained by chromatography on silica gel (20% ethyl acetate/hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05616596 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-7a6e7ff6416e4d33a0570bba9e53735b |
| Source note | uspto-grants-1997_04 |