HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 58598870, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 3729139 | HCID 3729139 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 58598870 | HCID 58598870 | — |
Reaction Steps
Thionyl chloride (1.9 mL, 26.4 mmol) was added to a solution of 2,2a,7,7a-tetrahydro-cyclobuta[a]inden-1-one oxime (1.5 g, 8.8 mmol) in 1,4-dioxane (44 mL), and stirred overnight at room temperature. The reaction was quenched with saturated aqueous NaHCO3 (100 mL), and extracted with EtOAc (3×50 mL). The organic extracts were washed with brine, dried over MgSO4, and concentrated to give the subtitle compound and its regioisomer, which were used without further purification. MS calculated for C11H11NO+H: 174, observed: 174.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07935830B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-cf48661b97354fa99b74da04b887814d |
| Source note | uspto-grants-2011_05 |