HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 53762272, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | [1-(2,3-Dimethoxybenzyl)cycloheptyl]methanol | HCID 19961173 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 53762272 | HCID 53762272 | 81% |
Reaction Steps
The alcohol from Step C above (25 g, 89 mmol) was dissolved in 500 mL of anhydrous DMSO. To this solution was added Et3N (50 mL, 358 mmol). Then SO3.Pyridine (57 g, 358 mmol), was dissolved in 400 mL of DMSO, and this solution was added to the reaction vessel. The solution was then stirred at room temperature for two hours. The reaction solution was then poured over ice and the resulting mixture was warmed to room temperature and extracted with CH2Cl2. The organic layer was washed with 1M HCl, water, and brine, then the organic layer was dried over MgSO4, filtered and evaporated. The crude product was chromatographed on silica gel, eluting with 10:1 hexane:EtOAc to give the title product as a colorless oil (20 g, 81% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05621133 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-34ae82ec46294e1f90e675899fae7f5e |
| Source note | uspto-grants-1997_04 |