HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexane → HCID 11805008, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3,5,6,7-tetrahydro-s-indacen-1(2H)-one | HCID 10931891 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 11805008 | HCID 11805008 | — |
Reaction Steps
The mixture of 3,5,6,7-tetrahydro-s-indacen-1(2H)-one (12.4 g, 0.072 mol), p-toluenesulfonyl hydrazide (13.4 g, 0.072 mol), 0.5 g TSA and i-propanol (100 ml) was refluxed by 5 min, and cooled to room temperature. Precipitate was filtered, washed by MeOH and dried, given 21 g of product (90%). Suspension of obtained hydrazone in 250 ml abs. Et2O was cooled to −70° C. and was treated with 15% n-butyllithium in hexane (100 ml. 0.16 mol). The resulting mixture was allowed to warm up to r.t. and refluxed until gas evolution. Reaction mixture was treated with 50 ml NH4Cl (10%), washed by water and dried. Solvent was evaporated, the residue was extracted by hot hexane, and to give after evaporation 9.1 g of solid product (81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08247587B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-1158f6394c2f40158f4c24daaae87586 |
| Source note | uspto-grants-2012_08 |