HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thioxanthone → 9-cyclopropyl-9H-thioxanthen-9-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thioxanthone | HCID 10295 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178418630 | HCID 178418630 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 9-cyclopropyl-9H-thioxanthen-9-ol | HCID 18799335 | — |
Reaction Steps
A solution of cyclopropylmagnesium bromide in dry THF (prepared from cyclopropylbromide (18.2 g, 0.15 mol), magnesium turnings (2.9 g, 0.12 mol) and dry THF (80 ml)) was placed under an atmosphere of nitrogen. A solution of thioxanthen-9-one (12.7 g, 0.06 mol) in dry THF (70 ml) was added dropwise and when addition was complete the mixture was heated at reflux for 20 minutes. The reaction mixture was cooled on an ice-bath and saturated ammonium chloride (70 ml) was carefully added. The mixture was diluted with water (100 ml) and extracted with diethyl ether (2×100 ml). The combined organic extracts were washed with water, dried (Na2SO4) and the solvent was evaporated in vacuo to give 25.2 g of crude 9-cyclopropyl-9H-thioxanthen-9-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05595989 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-19d9116f4a0740c0be5aae1d7fba87f3 |
| Source note | uspto-grants-1997_01 |