돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2122094생성일: 2026년 10월 27일

5-Decenoic acid → Dec-5-enyl acetate

https://huagongshe.com/reaction/2122094

반응식

참여 물질

역할이름HCID투입량
반응물5-Decenoic acidHCID 53400879—
반응물5-DecenoateHCID 74052926—
생성물Dec-5-enyl acetateHCID 38027—

반응 단계

For example, 5-hexenoic acid or an ester of 5-hexenoic acid (e.g. methyl 5-hexenoate, ethyl 5-hexenoate, etc . . . ) could be used instead of 1-hexene, but the synthesis would entail a reduction of a carboxylic acid or an ester to an alcohol followed by acetylation. These syntheses are respectively shown in FIGS. 12 and 13. With reference to FIGS. 12 and 13, the 5-hexenoic acid or 5-hexenoate is reacted with 5-decene to form 5-decenoic acid or 5-decenoate, respectively, in the presence of Catalyst 823 and under vacuum. The resulting 5-decenoic acid or 5-decenoate is reduced and acetylated to form 5-decenyl acetate. In addition, synthesizing 5-decenoic acid has advantages because the salt of 5-decenoic acid can be recrystallized to increase the trans-isomer to greater than 90 percent trans-5-decenoic acid, which is then reduced and acetylated to greater than 90 percent trans-5-decenyl acetate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06696597B2
출처 데이터셋uspto-grants-2004_02
ORD IDord-69cd3861e4484f95830302ca797ae4ac
출처 메모uspto-grants-2004_02