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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980624Generated: October 26, 2026

Ammonia → 7-Octenal

https://huagongshe.com/reaction/1980624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
Reactant7-OctenalHCID 88947—
ReactantOct-7-en-1-amineHCID 12878169—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product7-OctenalHCID 88947—
ProductHCID 20402326HCID 20402326—

Reaction Conditions

Temperature35 °C

Reaction Steps

A 100 ml autoclave with a magnetic stirrer was charged with 0.5 g of a Raney nickel catalyst (nickel content 53 weight %), 4 g of 7-octen-1-al, 20 g of ethanol, 4 g of water and 12 g of ammonia. Hydrogen was introduced into the autoclave at room temperature to 30 atmospheres. While maintaining the inside temperature at 35° C., the reaction was carried out with stirring. Approximately the theoretical amount of hydrogen was absorbed in 7 hours, when the reaction was stopped. The unreacted hydrogen and ammonia were released, and the liquid reaction mixture was analyzed by gas chromatography. It was revealed that the yield of 7-octenamine was 3.0 g (76% based on the charged 7-octen-1-al). As a byproduct, 0.4 g of the condensation product (Schiff base) of 7-octenamine with 7-octen-1-al was found and, when treated with diluted hydrochloric acid, yielded 7-octenamine hydrochloride and 7-octen-1-al; the 7 -octen-1-al forming the organic layer was separated and the aqueous layer was made basic with sodium hydroxide to give 0.2 g of 7-octenamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04510331
Source datasetuspto-grants-1985_04
ORD IDord-aa584c4d0eb74a1b880906916d6b3ba5
Source noteuspto-grants-1985_04