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HRID 64597作成日:2026年10月24日

Hydrochloric Acid → Gossyplure

https://huagongshe.com/ja/reaction/64597

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物1-Acetoxy-2-bromoethaneHCID 13564—
反応物Tetradeca-1,5,9-trieneHCID 54124585—
反応物HCID 178418265HCID 178418265—
触媒Titanium TetrachlorideHCID 24193—
生成物GossyplureHCID 536326511%

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04609498
出典データセットuspto-grants-1986_09
ORD IDord-84f5d1ced4764e9682f1afa69091250d
出典メモuspto-grants-1986_09