HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfide → 5,5-Dimethyl-2-phenylcyclopent-2-en-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 3,3-Dimethyl-1-phenylhex-5-en-2-one | HCID 15339370 | — |
| Reactant | Oxygen ozone | HCID 131711318 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5,5-Dimethyl-2-phenylcyclopent-2-en-1-one | HCID 12570669 | 79.6% |
Reaction Steps
A solution of the product of Step 2 (15 g) in 70 mL of MeOH and 50 mL of CH2Cl2 was treated with a stream of ozone/oxygen until the solution turned light blue. Dimethylsulfide (20 mL) was added and the reaction mixture was stirred for 2 h at room temperature and then treated with 5 g of triphenylphosphine for an additional 0.5 h. DBU (1 mL) was then added to the reaction mixture. After stirring for 1 h at room temperature, 1 mL of AcOH was added and the reaction mixture was concentrated. The residue was dissolved in 100 mL of 20:1 hexanes/EtOAc and the solution was filtered through a pad of silica gel. The filtrate was concentrated to give 11 g of the tite compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06222048B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-3ba58c157a474edda1f28edb5a1b4be2 |
| Source note | uspto-grants-2001_04 |