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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381725Generated: October 25, 2026

Triphenylphosphine → ethyl (Z)-dodec-5-enoate

https://huagongshe.com/reaction/1381725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1-BromoheptaneHCID 12369—
ReactantHeptyltriphenylphosphonium bromideHCID 2724567—
ReactantEthyl 5-oxopentanoateHCID 11137279—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Productethyl (Z)-dodec-5-enoateHCID 570889299.8%

Reaction Conditions

Temperature10 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04803289
Source datasetuspto-grants-1989_02
ORD IDord-aeab639ffcba491084e187063bd07349
Source noteuspto-grants-1989_02