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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301482Generated: October 29, 2026

Tributylstannane → HCID 17873231, compound

https://huagongshe.com/reaction/2301482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylstannaneHCID 5948—
ReactantAcrylonitrileHCID 7855—
Reactant1-Bromo-3,5-dimethyladamantaneHCID 98317—
Catalyst1,1'-Azobis(cyclohexanecarbonitrile)HCID 74978—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductHCID 17873231HCID 1787323186.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500866B1
Source datasetuspto-grants-2002_12
ORD IDord-a11b5cd4f7e347498f78dbc0b36981ea
Source noteuspto-grants-2002_12