HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127750Generated: October 25, 2026
1-Butanol → Butyl 3,7-dimethyl-8-oxoocta-2,4,6-trienoate
https://huagongshe.com/reaction/127750
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Formyl-crotonic acid butyl ester | HCID 86735241 | — |
| Solvent | Water | HCID 962 | — |
| Product | Butyl 3,7-dimethyl-8-oxoocta-2,4,6-trienoate | HCID 53845956 | — |
Reaction Steps
212.6 G. of 2-formyl-but-2-ene-4-triphenyl-phosphonium chloride and 95 g. of 3-formyl-crotonic acid butyl ester are introduced into 1100 ml. of butanol and treated at 5° C. with a solution of 57 g. of triethylamine in 60 ml. of butanol. The reaction mixture is subsequently stirred for 6 hours at 25° C., then cooled and introduced into water and thoroughly extracted with hexane. The hexane phase is washed first repeatedly with methanol/water (6:4 parts by volume), then with water, dried over sodium sulphate and filtered. The filtrate is isomerized for 12 hours by shaking with iodine. The iodine is removed by the addition of sodium thiosulphate. The filtrate is washed again with water, dried and evaporated under reduced pressure. The remaining 7-formyl-3-methyl-octa-2,4,6-trien-1-oic acid butyl ester boils, after rectification, at 102°-105° C./0.09 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04256878 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-016d90f705054688b3bbb6921d505e4c |
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| Source note | uspto-grants-1981_03 |
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