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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27849생성일: 2026년 10월 23일

1,2-Epoxybutane → 3,7-Dimethyl-nona-2,4,6,8-tetraen-1-oic acid butyl ester

https://huagongshe.com/ko/reaction/27849

반응식

참여 물질

역할이름HCID투입량
반응물1,2-EpoxybutaneHCID 7834—
반응물Butyl 3,7-dimethyl-8-oxoocta-2,4,6-trienoateHCID 53845956—
반응물3-Chloro-2,4,6-trimethyl-benzyl-triphenylphosphonium chlorideHCID 86735897—
생성물3,7-Dimethyl-nona-2,4,6,8-tetraen-1-oic acid butyl esterHCID 54292054—

반응 단계

16 g of 3-chloro-2,4,6-trimethyl-benzyl-triphenylphosphonium chloride and 10 g of 7-formyl-3-methyl-octa-2,4,6-trien-1-oic acid butyl ester are heated to boiling with stirring after the addition of 40 g of 1,2-butylene oxide. The 1,2-butylene oxide is slowly distilled off. The reaction mixture is stirred for 30 minutes at 80°-82° C., then cooled and thoroughly extracted with hexane. The hexane extract is shaken out 5 times with 50 ml of methanol/water 70:30 parts by volume each time, then dried over sodium sulphate and evaporated under reduced pressure to produce 9-(3-chloro-2,4,6-trimethyl-phenyl), 3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid butyl ester as a residue.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04224244
출처 데이터셋uspto-grants-1980_09
ORD IDord-5a0510b3ae024dbeafefae45eb02d3e0
출처 메모uspto-grants-1980_09