HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 15097264, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (3,4-Dihydro-2H-pyran-6-yl)methanol | HCID 12511647 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15097264 | HCID 15097264 | 112,043.602% |
Reaction Steps
51.5 g (0.45 mol) of methanesulfonyl chloride are added dropwise to 45 g (0.39 mmol) of 6-hydroxymethyl-2,3-dihydropyran (Example 7a) and 50 g (0.5 mol) of triethylamine in 400 ml of methylene chloride at 0°-5° C. Stirring is carried out for 1 hour at 0° C. and the reaction mixture is poured onto water. The aqueous phase is separated off and the organic phase is extracted once again with water and is then dried over MgSO4 and evaporated down. 84 g of title compound are obtained as a red oil, which is used directly in the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05536734 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-08fa25b7548a4995a978190d9a944685 |
| Source note | uspto-grants-1996_07 |