HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylstannane → HCID 17873231, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | 1-Bromo-3,5-dimethyladamantane | HCID 98317 | — |
| Catalyst | 1,1'-Azobis(cyclohexanecarbonitrile) | HCID 74978 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 17873231 | HCID 17873231 | 86.3% |
Reaction Steps
A solution of 1-bromo-3,5-dimethyladamantane (1.0 g, 4.11 mmol), acrylonitrile (436 mg, 8.22 mmol) and 1,1′-azobis(cyclohexanecarbonitrile) (50 mg, 0.21 mmol) in dry toluene (12 mL) was treated with tri-n-butyltin hydride (1.44 g, 4.93 mmol) at room temperature, refluxed for 3.5 h, cooled, diluted with ether (30 mL), washed with 0.2-M NH4OH (30 mL), water (10 mL), dried (MgSO4) and concentrated in vacuo. The residue was purified by chromatography [SiO2, CH2Cl2-hexane (0:100 to 100:0)] to give the product (771 mg, 86%) as a colourless oil: IR νmax (liquid film)/cm−1 2899, 2841, 2247, 1545 and 1359; NMR δH (400 MHz, CDCl3) 0.81 (6H, s), 1.0-1.2 (6H, m), 1.25-1.35 (6H, m), 1.53 (2H, t, J 4.2 Hz), 2.05-2.10 (1H, m) and 2.27 (2H, tJ 4.2 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06500866B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-a11b5cd4f7e347498f78dbc0b36981ea |
| Source note | uspto-grants-2002_12 |