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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 221111생성일: 2026년 10월 24일

1,1-Dibromoethane → Tributyl-(4-ethylphenyl)stannane

https://huagongshe.com/ko/reaction/221111

반응식

참여 물질

역할이름HCID투입량
반응물1,1-DibromoethaneHCID 11201—
반응물Tributyltin ChlorideHCID 15096—
반응물1-Bromo-4-ethylbenzeneHCID 15313—
반응물Potassium FluorideHCID 522689—
반응물MagnesiumHCID 5462224—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물Tributyl-(4-ethylphenyl)stannaneHCID 6004126792.9%

반응 단계

To a solution of magnesium (896 mg) in tetrahydrofuran (20 ml) was added dibromoethan (0.1 ml), and the mixture was stirred at room temperature for 15 minutes. Thereto was added dropwise a solution of 1-bromo-4-ethylbenzene (5.7 g) in tetrahydrofuran (20 ml), and subsequently, the mixture was stirred at room temperature for one hour. The reaction mixture was cooled to −78° C., and thereto was added dropwise tributyltin chloride (9.49 g). The mixture was stirred at the same temperature for 30 minutes, and then at room temperature for one hour. To the reaction mixture were added 10% aqueous potassium fluoride solution and ethyl acetate, and the mixture was stirred at room temperature for 30 minutes. Insoluble materials were filtered off. The organic layer of the filtrate was washed with water and brine successively, and dried over sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by alumina column chromatography (hexane) to give the desired tri-n-butyl(4-ethylphenyl)tin (10.7 g) as colorless oil. EI-Mass m/Z 337 (M-Bu).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202984B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-8fc2004b953e4e50b62929aa4fd2ac9a
출처 메모uspto-grants-2012_06