HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Epoxybutane → HCID 54347864, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Epoxybutane | HCID 7834 | — |
| Reactant | Ethyl 3,7-dimethyl-8-oxoocta-2,4,6-trienoate | HCID 54295620 | — |
| Reactant | HCID 86735150 | HCID 86735150 | — |
| Product | HCID 54347864 | HCID 54347864 | — |
Reaction Steps
39 g. of 2,6-dichloro-4-methoxy-benzyl-triphenylphosphonium chloride and 16 g. of 7-formyl-3-methyl-octa-2,4,6-trien-1-oic acid ethyl ester are heated at 82°-85° C. under reflux conditions while stirring for 2 hours after the addition of 40 g. of 1,2-butylene oxide. The mixture is then thoroughly extracted with hexane. The hexane extract is washed several times with methanol/water (60:40 parts by volume), dried over sodium sulphate and evaporated under reduced pressure. The residue is purified by absorption on silica gel using hexane for the elution. The 9-(2,6-dichloro-4-methoxyphenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid ethyl ester obtained from the eluate melts at 117°-118° C. after recrystallization from hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04054589 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-fc1ebbf9d9704c6e88ed8abb91c3281f |
| Source note | uspto-grants-1977_10 |