HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylstannane → HCID 22507637, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Heptane | HCID 8900 | — |
| Reactant | 12-Bromo-1-dodecanol | HCID 137895 | — |
| Reactant | Bis(1-hydroxy-2,2,6,6-tetramethyl-4-piperidinyl)decandioate | HCID 11272241 | — |
| Reactant | Ethylacetate heptane | HCID 21899848 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | HCID 22507637 | HCID 22507637 | — |
Reaction Steps
Tributyltin hydride is added dropwise to a solution of 12-bromo-1-dodecanol and excess bis(1-oxyl-2,2,6,6-tetramethylpiperidin-4-yl) sebacate in chlorobenzene. The mixture is heated to facilitate reaction. The crude reaction mixture is passed through silica gel with heptane and then heptane/ethyl acetate to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06872832B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-270ebdf2cfbf45d1a6edfcda8d33a080 |
| Source note | uspto-grants-2005_03 |