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HRID 862069作成日:2026年10月26日

Water → (4-Methoxymethoxy-phenylethynyl)-trimethylsilane

https://huagongshe.com/reaction/862069

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物ChlorotrimethylsilaneHCID 6397—
反応物4-(2,2-Dibromoethenyl)phenol methoxymethyl etherHCID 54096825—
反応物HCID 178418244HCID 178418244—
溶媒TetrahydrofuranHCID 8028—
生成物(4-Methoxymethoxy-phenylethynyl)-trimethylsilaneHCID 10657368—

反応手順

A solution of 4-(2,2-dibromoethenyl)phenol methoxymethyl ether (16.56 g) in THF (350 ml) was cooled to -78° C., to which was added dropwise, under argon atmosphere, a 1.6M n-butyl lithium hexane solution (70 ml). The mixture was stirred for one hour under the same conditions, which was then warmed and stirred for one hour at room temperature. The reaction mixture was cooled with ice, to which was added dropwise trimethylchlorosilane (7.2 ml). The mixture was then stirred for 3 hours while warming up to room temperature, to which was added water to quench the reaction, followed by extraction with ethyl acetate. The organic layer was washed (a saturated aqueous saline solution) and dried (anhydrous magnesium sulfate), then the solvent was distilled off under reduced pressure. The residue was purified by means of a silica gel column chromatography (eluted with ethyl acetate/hexane) to give 4-(2-trimethylsilylethynyl)phenol methoxymethyl ether (10.76 g) (Compound B-26). The physical properties are shown in Table 8.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05716971
出典データセットuspto-grants-1998_02
ORD IDord-6b044bd90cf64d54978473a34cffc4cc
出典メモuspto-grants-1998_02