HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dibromomethane → HCID 86657577, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dibromomethane | HCID 3024 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | 2-Phenylacetophenone | HCID 9948 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86657577 | HCID 86657577 | 89.6% |
Reaction Steps
To a solution of 1,2-diphenylethanone (10.0 g, 51.0 mmol) in anhydrous THF (100 mL) was added KOtBu (1M in THF, 51.0 mL, 51.0 mmol). The mixture was stirred for 30 min at room temperature, and carbon disulfide (7.76 g, 102 mmol) was added. After 10 min, dibromomethane (17.72 g, 102 mmol) was added and the reaction was stirred for 4 h at room temperature. The reaction was quenched with water (10 mL) and diluted with EtOAc. The organic layer was separated, dried over MgSO4, and concentrated to give the title compound as a yellow solid (13.0 g). LCMS m/z=285.0 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09012478B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-3695c2aaa0fc427ebd9b674927be5154 |
| Source note | uspto-grants-2015_04 |