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HRID 73472作成日:2026年10月25日

2-Phenyl-1,3-dithiane → Chlorodiethyl(2-phenyl-1,3-dithian-2-yl)germanium

https://huagongshe.com/reaction/73472

反応式

関与物質

役割名称HCID仕込み量
反応物2-Phenyl-1,3-dithianeHCID 21547—
反応物DichlorodiethylgermaneHCID 83334—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物Chlorodiethyl(2-phenyl-1,3-dithian-2-yl)germaniumHCID 86634585—

反応条件

温度-10 °C

反応手順

19.63 g (0.10 mol) 2-phenyl-1,3-dithian was dissolved under argon in 200 ml anhydrous tetrahydrofuran (THF) in a dry 500-ml three-necked flask with 50 ml dropping funnel, internal thermometer, magnetic stirrer and septum. The solution was cooled to −10° C. 44 ml of a 2.5 molar solution of n-butyllithium (0.11 mol) in n-hexane was added dropwise at −5° C. over a period of 50 min. After the addition was complete, the green solution was stirred for 2 h at 0° C. It was then added dropwise within 45 min to a solution, cooled to −72° C., of 20.16 g (0.10 mol) diethylgermanium dichloride in 500 ml anhydrous THF, wherein the temperature did not exceed −65° C. The reaction mixture was stirred for a further 16 h in a thawing cold bath, then concentrated on the rotary evaporator. 100 ml dry n-hexane was added to the residue followed by stirring for 1 h at room temperature. The suspension was filtered and the filtrate was concentrated on the rotary evaporator and dried under fine vacuum. The oily, yellow crude product was purified by means of high-vacuum distillation (b.p.: 135-150° C./4×10−5 mbar). 27.23 g (75% of the theoretical value) chlorodiethyl(2-phenyl-1,3-dithian-2-yl)germanium was obtained as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08829067B2
出典データセットuspto-grants-2014_09
ORD IDord-3df9e9425e1042579735a9497a7af661
出典メモuspto-grants-2014_09