HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Cyclopropylmethyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Cyclopropanemethanol | HCID 75644 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Cyclopropylmethyl methanesulfonate | HCID 135444 | 104.2% |
Reaction Steps
Cyclopropylcarbinol (27.4 g; 0.373 mol) and methanesulfonyl chloride (47.56 g; 0.407 mol) in dry ether (250 ml) was cooled to -20° C. under dry nitrogen. Triethylamine (59 ml; 0.42 mol) is added dropwise over 45 min with external cooling so that the reaction temperature remained below -15° C. The reaction mixture was allowed to warm to room temperature over 2 h and then filtered. The solid material is washed with ether. The solutions were combined and evaporated, to afford crude cyclopropylmethyl methanesulfonate (58.36 g) as a pale yellow liquid, which was used without further purification. NMR - d(CDCl3 ; 60 MHz) 0.3-1.5 (5H, m), 3.0 (3H, s) and 4.0 (2H, d, J=7 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05308830 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-bf6ec68de33642ea8225a76689be6fe0 |
| Source note | uspto-grants-1994_05 |