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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231004Generated: October 25, 2026

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

https://huagongshe.com/reaction/231004

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 (16.8g), 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 1.7 M 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 (8.6g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04844892
Source datasetuspto-grants-1989_07
ORD IDord-7d3e9c20adec4602852dfb9f2df8d5ea
Source noteuspto-grants-1989_07