HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Ethyl-2-(mesyloxymethyl)hexanal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-Ethyl 2-(hydroxymethyl)hexanal | HCID 12538467 | — |
| Product | 2-Ethyl-2-(mesyloxymethyl)hexanal | HCID 11572217 | 103.4% |
Reaction Steps
To a cold (10° C.) solution of 12.6 g (0.11 mole) of methanesulfonyl chloride and 10.3 g (0.13 mole) of triethylamine was added dropwise 15.8 g of 2-ethyl-2-(hydroxymethyl)hexanal, prepared according to the procedure described in Chem. Ber. 98, 728-734 (1965), while maintaining the reaction temperature below 30° C. The reaction mixture was stirred at room temperature for 18 h, quenched with dilute HCl and extracted with methylene chloride. The methylene chloride extract was dried over MgSO4 and concentrated in vacuo to give 24.4 g of brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06642268B2 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-9d8f86e80095481784dd189bdd722cb9 |
| Source note | uspto-grants-2003_11 |