HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylstannane → Ethyl 2-(2-chlorocyclopropyloxyimino)-3,3-ethylenedioxybutyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | HCID 53818524 | HCID 53818524 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 2-(2-chlorocyclopropyloxyimino)-3,3-ethylenedioxybutyrate | HCID 54085048 | 33.9% |
Reaction Steps
A solution of ethyl 2-(2,2-dichlorocyclopropyloxyimino)-3,3-ethylenedioxybutyrate (syn isomer)(312 mg) and tri-n-butyltinhydride (0.55 ml) in toluene (2 ml) was refluxed under nitrogen atmosphere in the presence of catalytic amount of 2,2'-azobisisobutyronitrile for 2 hours. The reaction mixture was concentrated in vacuo. The residue was subjected to column chromatography on silica gel (24 g) and eluted with a mixture of diethyl ether and n-hexane (1:2 V/V). The fractions containing the compound, which had higher Rf-value on TLC [development solvent system: diethyl ether and n-hexane (2:1 V/V)], were collected and concentrated in vacuo to give ethyl 2-(2-chlorocyclopropyloxyimino)-3,3-ethylenedioxybutyrate (syn isomer)(94 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04973699 |
| Source dataset | uspto-grants-1990_11 |
| ORD ID | ord-0976c6e08e6144738dba0b8f70d2efdc |
| Source note | uspto-grants-1990_11 |