HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylstannane → HCID 53837129, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | HCID 53926002 | HCID 53926002 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 53837129 | HCID 53837129 | 44.3% |
Reaction Steps
A solution of ethyl 2-(2-bromo-2-fluorocyclopropyloxy- imino)-3,3-ethylenedioxybutyrate (syn isomer)(4 g) and tri-n-butyltinhydride (2.28 ml) in benzene (30 ml) was refluxed under nitrogen atmosphere in the presence of 2,2'-azobisisobutyronitrile (250 mg) for 2 hours. The reaction mixture was concentrated in vacuo. The residue was subjected to column chromatography on silica gel and eluted with benzene. The fractions containing the compound, which had higher Rf-value on TLC [development solvent system:benzene], were collected and concentrated in vacuo to give ethyl 2-(2-fluorocyclopropyloxyimino)-3,3-ethylenedioxybutyrate (syn isomer)(1.36 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04861769 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-d8c4e92c91ff4fee825ef8b4018d4f5f |
| Source note | uspto-grants-1989_08 |