Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1,2-Epoxybutane → 3,7-Dimethyl-nona-2,4,6,8-tetraen-1-oic acid butyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1,2-Epoxybutane | HCID 7834 | — |
| 반응물 | Butyl 3,7-dimethyl-8-oxoocta-2,4,6-trienoate | HCID 53845956 | — |
| 반응물 | 3-Chloro-2,4,6-trimethyl-benzyl-triphenylphosphonium chloride | HCID 86735897 | — |
| 생성물 | 3,7-Dimethyl-nona-2,4,6,8-tetraen-1-oic acid butyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04224244 |
| 출처 데이터셋 | uspto-grants-1980_09 |
| ORD ID | ord-5a0510b3ae024dbeafefae45eb02d3e0 |
| 출처 메모 | uspto-grants-1980_09 |