HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylstannane → HCID 19887190, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | HCID 53802832 | HCID 53802832 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 19887190 | HCID 19887190 | — |
Reaction Steps
N-(2-Butenyl)-N-(3-trifluoromethylphenyl)-2-chloro-2-(3,5-difluorophenyl)acetamide (1.6 g) was added to 30 ml of benzene, followed by the addition of 1.1 ml of tributyltin hydride and a catalytic amount of α,α-azobisisobutyronitrile (AIBN) under stirring at the refluxing temperature. The reaction mixture was then stirred for 20 minutes at the refluxing temperature. The reaction mixture was then concentrated in an evaporator. The resultant concentrate was purified by chromatography on a silica gel, whereby 0.75 g of the 3,4-trans isomer of 4-ethyl-3-(3,5-difluorophenyl)-1-(3-trifluoromethylphenyl)-2-pyrrolidinone and 0.14 g of its 3,4-cis isomer were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05131947 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-386a28b0206b42b8adf262c3bd743bc4 |
| Source note | uspto-grants-1992_07 |