HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3,3-Dimethylbutyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3,3-Dimethyl-1-butanol | HCID 12233 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3,3-Dimethylbutyl methanesulfonate | HCID 19039459 | — |
Reaction Steps
To a stirred solution of 3,3-dimethyl-1-butanol (2 ml) in dichloromethane (48 ml), under nitrogen, was added triethylamine (4.64 ml) and the resulting solution cooled to 0/C. Methanesulphonylchloride (1.28 ml) was then added dropwise via syringe and stirring continued for 18 h as the reaction warmed to room temperature. The reaction was then concentrated onto silica and purified by flash chromatography to give the title compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05912252 |
| Source dataset | uspto-grants-1999_06 |
| ORD ID | ord-e27acd651a474426b355d3f6d72b6602 |
| Source note | uspto-grants-1999_06 |