戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 436108作成日:2026年10月26日

Iodine → 4,4-Dimethyl-1-iodo-trans-1-octen-3-ol

https://huagongshe.com/reaction/436108

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Sodium HydroxideHCID 14798—
反応物Sodium ThiosulfateHCID 24477—
反応物Ethanamine, N,N-diethyl-, N-oxideHCID 123168—
反応物Bis(1,2-dimethylpropyl)boraneHCID 192733—
反応物2-[(4,4-Dimethyloct-1-YN-3-YL)oxy]oxaneHCID 14516370—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒DiglymeHCID 8150—
生成物4,4-Dimethyl-1-iodo-trans-1-octen-3-olHCID 20465723—

反応手順

To 233 ml. of a 0.43M solution of disiamylborane in diglyme cooled to 0° C. under an inert atmosphere is added 23.8 g. (0.100 mole) 4,4-dimethyl-3-tetrahydropyranyloxy-1-octyne (Example 995). The mixture is allowed to come to room temperature and is stirred at ambient temperature for 3 hours. The solution is cooled to 0° C. and 22.5 g. (0.30 mole) of triethylamine oxide is added portionwise such that the temperature is maintained at 0°-5° C. The mixture is stirred at 0° C. for 1 hour and is then poured into 150 ml. of 1 N sodium hydroxide followed immediately by a solution of 25.4 g. (0.100 mole) of iodine in 60 ml. of tetrahydrofuran. The mixture is stirred at ambient temperatures for 0.5 hour and poured into 500 ml. of water. The mixture is decolorized by addition of sodium thiosulfate solution and is extracted into ether. The organic phase is washed with water and the solvent is removed in vacuo. The residue is stirred at room temperature for 20 hours with 900 ml. 3:1:1 tetrahydrofuran-acetic acid-water. The solution is evaporated in vacuo and the residue is chromatographed on silica gel in benzene using 10-20% ethylacetate in benzene.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04007210
出典データセットuspto-grants-1977_02
ORD IDord-a9562b68861d49efbae522135db3cf18
出典メモuspto-grants-1977_02