HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Pentanol → Triphenylsulfonium 2,4,6-triisopropylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Pentanol | HCID 6276 | — |
| Reactant | 3-Methyl-2-butanone | HCID 11251 | — |
| Reactant | Triphenylsulfonium methylsulfate | HCID 22995011 | — |
| Reactant | Sodium 2,4,6-triisopropylbenzoate | HCID 118556701 | — |
| Solvent | Water | HCID 962 | — |
| Product | Triphenylsulfonium 2,4,6-triisopropylbenzoate | HCID 131735631 | 80% |
Reaction Steps
A 1-L eggplant shaped flask was charged with 22.4 g of sodium 2,4,6-triisopropylbenzoate (prepared in Synthesis Example 1-2), 31.1 g of triphenylsulfonium methylsulfate, 90 g of methyl isopropyl ketone, 90 g of 1-pentanol, and 40 g of water, which were stirred at room temperature for 1 hour. The organic layer was separated from the reaction mixture and washed with water. After washing, the organic layer was concentrated by distilling off the solvent. The liquid concentrate was crystallized from 300 g of diisopropyl ether. The crystal precipitate was filtered and dried, obtaining the target compound, triphenylsulfonium 2,4,6-triisopropylbenzoate as white crystal. Amount 40.4 g, yield 80%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09348227B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-c896c67c342f48fa8f84747cf3535aa3 |
| Source note | uspto-grants-2016_05 |