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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64597Generated: October 25, 2026

Hydrochloric Acid → Gossyplure

https://huagongshe.com/reaction/64597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Acetoxy-2-bromoethaneHCID 13564—
ReactantTetradeca-1,5,9-trieneHCID 54124585—
ReactantHCID 178418265HCID 178418265—
CatalystTitanium TetrachlorideHCID 24193—
ProductGossyplureHCID 536326511%

Reaction Conditions

Temperature0 °C

Reaction Steps

1,5,9-Tetradecatriene (10 g, 0.052 mol), n-butylmagnesium chloride (24.8 mL of 2.5M in tetrahydrofuran; 0.062 mol) and titanium tetrachloride (0.52 g, 0.0027 mol) were stirred under an inert atmosphere at about 65° C. for about 4.5 hours. The reaction mixture was then cooled to 0° C. and cuprous bromide (0.14 g, 1.0 mmol) was added. 2-Bromoethyl acetate (6.9 mL, 0.063 mol) was then added dropwise and the mixture allowed to warm slowly to room temperature and stirred for several hours at room temperature. Reaction temperature was then raised to 60° C. for 4 hours before the mixture was cooled, acidified with aqueous HCl, then extracted with hexane. The hexane extract was washed with saturated sodium bicarbonate solution, dried over MgSO4, filtered and solvent removed on the rotary evaporator. GLC analysis of this crude reaction product indicated an 11% yield of gossyplure. It should be recognized that while this reaction represents successful production of gossyplure from 1,5,9 -tetradecatriene in one reaction vessel, the reaction parameters have not been optimized. Consequently, significantly improved yields of gossyplure can be expected upon optimization of various reaction parameters.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04609498
Source datasetuspto-grants-1986_09
ORD IDord-84f5d1ced4764e9682f1afa69091250d
Source noteuspto-grants-1986_09