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HRID 247659作成日:2026年10月26日

Iodine → Silafluofen

https://huagongshe.com/reaction/247659

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物MagnesiumHCID 5462224—
反応物Benzene, 4-(3-bromopropyl)-1-fluoro-2-phenoxy-HCID 11781825—
反応物Chloro(4-ethoxyphenyl)dimethylsilaneHCID 14014482—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物SilafluofenHCID 92430—

反応条件

温度10 °C

反応手順

A small crystal of iodine was added to a mixture of 0.75 g (0.0024 mole) of 1-bromo-3-(4-fluoro-3-phenoxyphenyl)propane and 0.11 g (0.0045 mole) of magnesium powder in 1 ml of tetrahydrofuran. This mixture was heated in a water bath for about three hours. After heating, the clear solution was light grey-brown in color. The solution was cooled to 10° C., and 0.51 g (0.0022 mole) of chloro(4-ethoxyphenyl)dimethylsilane was added. This mixture was stirred for one-half hour and was then heated for an hour. Following dilution with diethyl ether, the reaction mixture was washed successively with 10% hydrochloric acid and a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under reduced pressure, leaving a colorless oil weighing 0.95 g as the residue. This oil was purified using a Chromatotron (eluant=ethyl acetate/hexane (2:98)), producing (4-ethoxyphenyl)[3-(4-fluoro-3-phenoxyphenyl)propyl]dimethylsilane as a colorless oil. The proton and 13C nmr spectra were consistent with the proposed structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04709068
出典データセットuspto-grants-1987_11
ORD IDord-80c3c0f2de454f139919488c3c15e12a
出典メモuspto-grants-1987_11