HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → HCID 13176138, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Hydroxy-5-pentylcyclopent-2-en-1-one | HCID 13176131 | — |
| Catalyst | Quinine | HCID 3034034 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 13176138 | HCID 13176138 | 104.5% |
Reaction Steps
Into the same flask as used in Example 1, thiophenol (10 g), triethylamine (2 g), quinine (0.2 g), 2-n-pentyl-3-hydroxy-4-cyclopentenone (16.8 g) and toluene (30 g) were charged, and the mixture was stirred under a nitrogen stream at a temperature of 40° to 70° C. for 5 hours. After completion of the reaction, the mixture was treated and purified in the same manner as in Example 50 to obtain 2-n-pentyl-4-phenylthio-2-cyclopentenone (24.7 g). Yield, 95%. nD20 1.5706.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04665174 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-4132d1e1e12149ad9de706bb0f9bd7c5 |
| Source note | uspto-grants-1987_05 |