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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1820945생성일: 2026년 10월 25일

2-Phenyl-1,3-dithiane → HCID 86619319, 화합물

https://huagongshe.com/reaction/1820945

반응식

참여 물질

역할이름HCID투입량
반응물2-Phenyl-1,3-dithianeHCID 21547—
반응물DichlorodiethylgermaneHCID 83334—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물HCID 86619319HCID 86619319—

반응 조건

온도0 °C

반응 단계

1.85 g (9.42 mmol) 2 phenyl-1,3-dithian was placed in a dry 50-ml three-necked flask under argon and dissolved in 28 ml anhydrous THF. 3.99 ml 2.36 M BuLi solution in hexane was added dropwise at 0° C. and the reaction solution stirred for 2 h at 0° C. 0.83 mg (3.93 mmol) diethyldichlorogermanium dissolved in 8 ml anhydrous THF was added slowly dropwise at 0° C. to the reaction mixture and then stirred for an additional 2 h at 0° C. To complete the reaction a further solution of 2-phenyl-2-lithium-1,3-dithian (2.36 mmol) was prepared as described above and added dropwise at 0° C. to the reaction solution, which was then stirred for 18 h at 6° C. The reaction was quenched by the addition of 20 ml water and the raw product extracted with diethyl ether (3×30 ml). The combined organic phases were dried with Na2SO4 and the solvent drawn off at the rotary evaporator. The residue was separated off by column chromatography (petroleum ether: ethyl acetate=20:1). 1.42 g (70% of the theoretical value) diethylbis(2-phenyl-1,3-dithian-2-yl)germanium was obtained as colorless solid. DC (petroleum ether: ethyl acetate=20:1): Rf=0.51

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07605190B2
출처 데이터셋uspto-grants-2009_10
ORD IDord-dfa0e26209c041fd990b1fa90cd53abe
출처 메모uspto-grants-2009_10