HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylstannane → 2-Fluoro-4-pyridin-3-ylmethyl-benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | thiocarbonic acid O-[(4-cyano-3-fluoro-phenyl)-pyridin-3-yl-methyl]Ester O-phenyl Ester | HCID 88184430 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-Fluoro-4-pyridin-3-ylmethyl-benzonitrile | HCID 54380660 | — |
Reaction Steps
To a solution of thiocarbonic acid O-[(4-cyano-3-fluoro-phenyl)-pyridin-3-yl-methyl]ester O-phenyl ester (as described in Step A above) (0.5 g, 1.37 mmol) in benzene (2.0 mL) was added AIBN (0.18 g, 1.1 mmol) and tri-n-butyltinhydride (1.09 mL, 4.0 mmol) and the solution was heated to refluxed for 2 hr. The solvents were removed in vacuo to obtain the title compound after chromatography (silica gel, CH2Cl2:MeOH 99:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06284755B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-0f4ceab516944c9dbb440c7296c2a865 |
| Source note | uspto-grants-2001_09 |