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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704371Generated: October 30, 2026

Sodium Azide → 1-[4-(Heptyloxy)phenyl]methanamine

https://huagongshe.com/reaction/704371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
Reactantp-Heptyloxybenzyl chlorideHCID 14674285—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-[4-(Heptyloxy)phenyl]methanamineHCID 15115534103.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 1.25 g of sodium azide in 2.5 ml of water was added to a solution of 900 mg of p-chloromethyl(heptyloxy)benzene in 25 ml of N,N-dimethylformamide, and the mixture was stirred at 100° C. for 6 hours. After cooling, the reaction mixture was diluted with water, and the product was extracted with ether. The ether layer was washed in sequence with water and saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. A solution of the thus-obtained residual oil in 10 ml of tetrahydrofuran was added dropwise at 0° C. over 5 minutes to a suspension of 200 mg of lithium aluminum hydride in 15 ml of tetrahydrofuran. The resultant mixture was stirred at the same temperature for 1 hour and then at room temperature for 1 hour. Then, sodium sulfate decahydrate added to decompose the excess lithium aluminum hydride. The insoluble matter was filtered off, and the filtrate was concentrated under reduced pressure to give 860 mg of p-heptyloxybenzylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04987132
Source datasetuspto-grants-1991_01
ORD IDord-d7afed0f174d49d3bec44f483304f6be
Source noteuspto-grants-1991_01