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1,2-Epoxybutane → 3,7-Dimethyl-nona-2,4,6,8-tetraen-1-oic acid butyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,2-Epoxybutane | HCID 7834 | — |
| 反応物 | Butyl 3,7-dimethyl-8-oxoocta-2,4,6-trienoate | HCID 53845956 | — |
| 反応物 | 3-Chloro-2,4,6-trimethyl-benzyl-triphenylphosphonium chloride | HCID 86735897 | — |
| 生成物 | 3,7-Dimethyl-nona-2,4,6,8-tetraen-1-oic acid butyl ester | HCID 54292054 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04224244 |
| 出典データセット | uspto-grants-1980_09 |
| ORD ID | ord-5a0510b3ae024dbeafefae45eb02d3e0 |
| 出典メモ | uspto-grants-1980_09 |