HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Thienylmethyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| 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
2-thienylmethanol mesylate is prepared by treating a solution of 2-thienylmethanol (5.57 g; 50 mmol) in methylene chloride (100 ml) and triethylamine (15.05 g, 150 mmol) at 0° C. with methanesulfonyl chloride (11.45 g, 100 mmol) dropwise and at RT 1 hr after the addition. The reaction mixture is poured into ice-water and the organic layer is separated, dried (MgSO4), and evaporated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08017622B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-3ab08de018f1492aac5067dd9cc82f13 |
| Source note | uspto-grants-2011_09 |