HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylstannane → HCID 13168697, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | 1-Methoxy-1-buten-3-yne | HCID 643188 | — |
| Product | HCID 13168697 | HCID 13168697 | — |
Reaction Steps
Scheme D shows a method of preparing an aldehyde which may be used in Scheme A. 1-Methoxy-1E-buten-3-yne is reacted with tributylstannane in the presence of catylytic 2,2'-azobisisobutyronitrile (AIBN) to give tributyl(4-methoxy-1E,3E-butadienyl)stannane which is then reacted with butyllithium followed by coupling with an appropriate aldehyde (XVIII). The alcohol-formed is reacted with toluene sulfonic acid (TSOH) to give the desired aldehyde (V).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05990326 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-ea0d9129f3764ca49791278c110764c1 |
| Source note | uspto-grants-1999_11 |