HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (R)-glycidyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (-)-Glycidol | HCID 6973630 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (R)-glycidyl methanesulfonate | HCID 12461091 | — |
Reaction Steps
A solution of (S)-(−)-glycidol (8.6 mL, 130 mmol) and triethylamine (36.2 mL, 260 mmol, 2.0 equiv.) in DMF (250 mL) was cooled over an ice bath and methanesulfonyl chloride (10.1 mL, 130 mmol, 1.0 equiv.) was added dropwise. The mixture was stirred for 1.5 hr at room temperature affording a 0.47 M solution of (R)-glycidyl methanesulfonate in DMF, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08895549B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-2f9adc3493324321b07976fe9d19e93a |
| Source note | uspto-grants-2014_11 |