HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 22381912, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Cyclobutylcarbinol | HCID 78130 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 22381912 | HCID 22381912 | 103.4% |
Reaction Steps
Cyclobutanemethanol (24.9 g; 0.287 mol) and methanesulfonyl chloride (35.3 g; 0.302 mol) in dry ether (250 ml) was cooled to -20° C. under dry nitrogen. Triethylamine (44 ml; 0.32 mol) was added dropwise over 15 min with external cooling so that the reaction temperature remained below -5° C. The reaction mixture was allowed to warm to room temperature over 1 h and then filtered. The remaining solid was washed with ether. The ether solutions were combined and the ether evaporated, to afford crude cyclobutylmethyl methanesulfonate (48.75 g) as a pale yellow liquid, which was used in the next step without further purification. NMR - d(CDCl3 ; 60 MHz) 1.6-2.9 (7H, m), 3.0 (3H, s) and 4.1 (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-78572052a87842bdaea973ef1123dcfb |
| Source note | uspto-grants-1994_05 |