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HRID 1975548作成日:2026年10月27日

Water → (5,5-Dimethyl-1,3-hexadiynyl)tri-n-butylstannane

https://huagongshe.com/reaction/1975548

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Tributyltin ChlorideHCID 15096—
反応物t-Butyl-1,3-butadiyneHCID 11423565—
反応物HCID 178418443HCID 178418443—
溶媒Diethyl EtherHCID 3283—
生成物(5,5-Dimethyl-1,3-hexadiynyl)tri-n-butylstannaneHCID 1910026339.7%

反応条件

温度-78 °C

反応手順

(5,5-dimethyl-1,3-hexadiynyl)tri-n-butylstannane was synthesized as follows a solution containing ethylmagnesium bromide (19.3 millimoles) and 5,5-dimethyl-1,3hexadiyne (19.3 millimoles) in 50 milliliters of ether was refluxed for 5 hours under nitrogen, then cooled to -78° C. To this solution, 18.6 millimoles of tri-n-butyltin chloride in 10 milliliters of ether was added slowly. The reaction mixture was allowed to warm to room temperature and stirred for 16 hours. Water was added to form a two-phase mixture, the phases were separated, and the aqueous phase was washed with ether. The ether wash was combined with the organic phase from the initial phase separation, and evaporated under reduced pressure to yield a crude oil. Distillation in vacuo produced 2.92 grams of pure (5,5-dimethyl-1,3-hexadiynyl)tri-n-butylstannane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05286901
出典データセットuspto-grants-1994_02
ORD IDord-5d0b42673f9040a9a73fcb9f5ab5eaeb
出典メモuspto-grants-1994_02