HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylstannane → (1,1-Dimethylethyl)(((2-(2,2-dimethylpropyl)-2'-fluoro-5'-(methyloxy)-1,1'-biphenyl-4-yl)methyl)oxy)dimethylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | HCID 57706174 | HCID 57706174 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (1,1-Dimethylethyl)(((2-(2,2-dimethylpropyl)-2'-fluoro-5'-(methyloxy)-1,1'-biphenyl-4-yl)methyl)oxy)dimethylsilane | HCID 57706342 | 94.6% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
To a stirred solution of 69.16B (0.015 g, 0.033 mmol) in toluene (2.00 mL) at 23° C. was added AIBN (0.00055 g, 0.0033 mmol) followed by tri-n-butyltin hydride (0.048 g, 0.17 mmol). The reaction was stirred at 100° C. for two hours. After which, the reaction was cooled to room temperature and concentrated in vacuo. The product was then purified on silica gel (0-10% EtOAc in hexanes) to yield 69.16D as a colorless oil (0.013 g, 94% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08030354B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-12689a3627a04cbeb035459f081d0953 |
| Source note | uspto-grants-2011_10 |