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HRID 367306作成日:2026年10月24日

(5-Carboxypentyl)triphenylphosphanium bromide → HCID 53684295、化合物

https://huagongshe.com/ja/reaction/367306

反応式

関与物質

役割名称HCID仕込み量
反応物(5-Carboxypentyl)triphenylphosphanium bromideHCID 2779280—
反応物HCID 23288036HCID 23288036—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 53684295HCID 5368429543%

反応手順

Under a nitrogen atmosphere, a solution of 0.92 g of potassium t-butoxide in 10 ml of THF was added dropwise to a suspension of 0.46 g of 5-carboxypentyltriphenylphosphonium bromide in 5 ml of THF at 0° C., and the mixture was stirred for 30 minutes. To the reaction solution was added dropwise a solution of 4,6-di-t-butyl-2-formyl-2-methyl-5-trimethylsilyloxy-2,3-dihydrobenzofuran synthesized in Example 72-2) in 10 ml of THF, and the mixture was stirred overnight while slowly warming to room temperature. The reaction solution was extracted with water and diethyl ether, and the combined aqueous layers were acidified with concentrated hydrochloric acid and extracted with diethyl ether. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography eluting with n-hexane containing 50% ethyl acetate to give 0.22 g of 6-(4,6-di-t-butyl-5-hydroxy-2-methyl-2,3-dihydrobenzofuran-2-yl)-5-hexenoic acid as a colorless viscous liquid (yield 43%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06133279
出典データセットuspto-grants-2000_10
ORD IDord-9301289ae4924d06bc13c186d034667f
出典メモuspto-grants-2000_10