関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Tributyltin Chloride | HCID 15096 | — |
| 反応物 | t-Butyl-1,3-butadiyne | HCID 11423565 | — |
| 反応物 | HCID 178418443 | HCID 178418443 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | (5,5-Dimethyl-1,3-hexadiynyl)tri-n-butylstannane | HCID 19100263 | 39.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05286901 |
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| 出典データセット | uspto-grants-1994_02 |
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| ORD ID | ord-5d0b42673f9040a9a73fcb9f5ab5eaeb |
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| 出典メモ | uspto-grants-1994_02 |
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