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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1980624생성일: 2026년 10월 27일

Ammonia → 7-Octenal

https://huagongshe.com/reaction/1980624

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Hydrochloric AcidHCID 313—
반응물7-OctenalHCID 88947—
반응물Oct-7-en-1-amineHCID 12878169—
반응물HCID 178418361HCID 178418361—
촉매NickelHCID 935—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물7-OctenalHCID 88947—
생성물7-Octenamine hydrochlorideHCID 20402326—

반응 조건

온도35 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04510331
출처 데이터셋uspto-grants-1985_04
ORD IDord-aa584c4d0eb74a1b880906916d6b3ba5
출처 메모uspto-grants-1985_04