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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814825Generated: November 2, 2026

Hexane → HCID 21973146, compound

https://huagongshe.com/reaction/1814825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
ReactantTrimethylaluminumHCID 16682925—
Reactant5-Benzyloxy-2-ethoxybenzonitrileHCID 21973169—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 21973146HCID 21973146—

Reaction Conditions

Temperature2.5 °C

Reaction Steps

46.46 g of ammonium chloride (868.5 mol) are suspended in 650 ml of toluene, and the mixture is cooled to 0-5° C. Trimethylaluminum is added dropwise as a 2M solution in hexane (445 ml, 888.3 mmol), and the mixture is then stirred at room temperature until the evolution of gas has ceased. 5-Benzyloxy-2-ethoxybenzonitrile (100 g, 394.8 mmol) (example 32A) is added, and the mixture is stirred at 80° C. overnight. The cooled reaction mixture is, with ice-cooling, added to a suspension of 200 g of silica gel and 2 l of dichloromethane, and the mixture is stirred for 30 min. The mixture is filtered off with suction and the filter cake is washed with methanol. The organic phases are combined and concentrated. The resulting residue is triturated using a mixture of dichloromethane/methanol 9:1, filtered and concentrated using a rotary evaporator. The residue is then triturated with ether, and the colorless solid is filtered off with suction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878708B2
Source datasetuspto-grants-2005_04
ORD IDord-d58d186105994bd6961aacecc5b80d80
Source noteuspto-grants-2005_04