HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 57259263, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | 17-Allyl-1-hydroxy-12-[2-(4-hydroxy-3-methoxycyclohexyl)-1-methylvinyl]-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9]octacosa-14,18-diene-2,3,10,16-tetraone | HCID 57153457 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 57259263 | HCID 57259263 | — |
Reaction Steps
To a stirred solution of 17-Allyl-1-hydroxy-12-[2-(4-hydroxy-3-methoxycyclohexyl)-1-methylvinyl]-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9 ]octacos-14,18-diene-2,3,10,16-tetraone (as prepared in Example 14) (100 mg) in toluene (5 ml) and acetic acid (0.01 ml) was added tetrakis(triphenylphosphine) palladium(0) (0.01 g). After 5 minutes tri n-butyltin hydride (0.04 g) was added and the reaction mixture was stirred at room temperature for 2 hours. Water was added and the reaction mixture was extracted with ether. The ether extracts were dried (magnesium sulphate), filtered and evaporated to an oil in vacuo. Chromatography on silica eluting with ether gave the title compound as a low melting solid (70 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05376663 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-7c50727033e94c1ca8143316d2e186f0 |
| Source note | uspto-grants-1994_12 |