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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28104생성일: 2026년 10월 24일

1,2-Epoxybutane → 9-(2,6-Dichloro-4-methoxy-5-methyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid ethyl ester

https://huagongshe.com/ko/reaction/28104

반응식

참여 물질

역할이름HCID투입량
반응물1,2-EpoxybutaneHCID 7834—
반응물TriphenylphosphineHCID 11776—
반응물2,6-Dichloro-4-methoxy-3-methyl-benzyl chlorideHCID 23462577—
반응물Ethyl 3,7-dimethyl-8-oxoocta-2,4,6-trienoateHCID 54295620—
반응물(2,6-Dichloro-3-methyl-4-methoxybenzyl) triphenyl phosphonium chlorideHCID 86736665—
용매Toluene hexaneHCID 21889329—
생성물9-(2,6-Dichloro-4-methoxy-5-methyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid ethyl esterHCID 127591—

반응 단계

100 g. of 2,6-dichloro-4-methoxy-5-methyl-benzyl-triphenylphosphonium chloride, prepared from 52 g. of 2,6-dichloro-4-methoxy-3-methyl-benzyl chloride and 57 g. of triphenylphosphine, are treated with 42 g. of 7-formyl-3-methyl-octa-2,4,6-trien-1-oic acid ethyl ester. After the addition of 120 ml. of 1,2-butylene oxide, the resulting mixture is heated to 80°-85° C. for 4 hours while stirring. The mixture is diluted with toluene/hexane (1:1 parts by volume) and exhaustively extracted with methanol/water (60:40 parts by volume). The resulting solution is evaporated under reduced pressure. The oily residue is purified by adsorption on silica gel using toluene for the elution. 9-(2,6-dichloro-4-methoxy-5-methyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid ethyl ester is obtained from the eluate and melts at 100°-101° C. after recrystallization from benzene/hexane (50:50 parts by volume).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04225527
출처 데이터셋uspto-grants-1980_09
ORD IDord-c89e883b75a84e41afb4b1f8004b6ddf
출처 메모uspto-grants-1980_09