Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972259Generated: October 29, 2026

4-(4-Chlorophenoxy)aniline → HCID 68705038, compound

https://huagongshe.com/reaction/1972259

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Chlorophenoxy)anilineHCID 7578—
Reactant3-BenzyloxybenzaldehydeHCID 74342—
ReactantTrimethylsilyl cyanideHCID 82115—
CatalystIodineHCID 807—
SolventMethanolHCID 887—
ProductHCID 68705038HCID 6870503867.3%

Reaction Steps

Reference to α-amino nitrile synthesis: Synlett, 2005, 8, 1325. A methanol solution (50 mL) of 3-benzyloxybenzaldehyde (5 g, 23.6 mmol), 4-amino-4-chlorodiphenyl ether (5.7 g, 25.9 mmol), iodine (120 mg, 0.47 mmol) and trimethylsilylcyanide (3.8 mL, 28.3 mmol) is stirred at room temperature for 18 h. The precipitate that formed is collected and rinsed with ethyl acetate/hexane (1:4) to obtain ˜7 g (67%) of 2-(4-(4-chlorophenoxy)phenylamino)-2-(3-(benzyloxy)phenyl)acetonitrile as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431607B2
Source datasetuspto-grants-2013_04
ORD IDord-0afec78f78d74b47b54f3d56cffa7041
Source noteuspto-grants-2013_04