HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381725Generated: October 25, 2026
Triphenylphosphine → ethyl (Z)-dodec-5-enoate
https://huagongshe.com/reaction/1381725
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1-Bromoheptane | HCID 12369 | — |
| Reactant | Heptyltriphenylphosphonium bromide | HCID 2724567 | — |
| Reactant | Ethyl 5-oxopentanoate | HCID 11137279 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | ethyl (Z)-dodec-5-enoate | HCID 5708892 | 99.8% |
Reaction Steps
Heptyltriphenylphosphonium bromide (16.8 g), prepared from 1-bromoheptane and triphenylphosphine analogously to undecyltriphenylphosphonium bromide as described in Example 2(2), is suspended in dry ether (300 ml) and the mixture is treated whilst stirring under nitrogen with 1.7M butyllithium in hexane (36 ml) from a syringe. The resulting bright red solution is cooled to 10° C. and treated dropwise with ethyl 5-oxopentanoate [5.5 g, prepared as described in Example 2 (1B)] in dry ether (37.5 ml). After 10 minutes, the reaction mixture is worked up by the procedure described in Example 2(2) to give ethyl (Z)-dodec-5-enoate as a yellow oil (8.6 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04803289 |
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| Source dataset | uspto-grants-1989_02 |
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| ORD ID | ord-aeab639ffcba491084e187063bd07349 |
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| Source note | uspto-grants-1989_02 |
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