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HRID 127075作成日:2026年10月27日

Iodine → 1-Iodo-4-trimethylsiloxy-trans-1-octene

https://huagongshe.com/reaction/127075

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Trimethylamine oxideHCID 1145—
反応物Sodium HydroxideHCID 14798—
反応物Bis(1,2-dimethylpropyl)boraneHCID 192733—
反応物Trimethyl[(oct-1-yn-4-yl)oxy]silaneHCID 12786181—
溶媒TetrahydrofuranHCID 8028—
生成物1-Iodo-4-trimethylsiloxy-trans-1-octeneHCID 12851277—

反応手順

To a stirred solution of 0.20 moles of freshly prepared bis-(3-methyl-2-butyl)borane in 300 ml of tetrahydrofuran at 0°-5° C. is added dropwise a solution of 19.8 g of 4-trimethylsiloxy-1-octyne in 30 ml of tetrahydrofuran. The resulting mixture is stirred at ambient temperature for several hours, cooled in an ice bath, and treated with 53 g of trimethylamine oxide. The mixture is stirred several hours at 25°-40° C. and then poured into 2 liters of 15% sodium hydroxide. The resulting mixture is treated immediately with a solution of 140 g of iodine in 300 ml of tetrahydrofuran. After 0.5 hour the organic phase is separated and the aqueous phase is extracted with ether. The combined organic layers are washed with water, sodium thiosulfate solution, and brine; dried over magnesium sulfate; and concentrated to give an oil pmr spectrum (CDCl3): 6.2 (d, ICH=) and 6.7 (quintuplet, =CH--).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04254285
出典データセットuspto-grants-1981_03
ORD IDord-cd53418e1b744ba4a3003cd35c9a0eb4
出典メモuspto-grants-1981_03