関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Iodine | HCID 807 | — |
| 反応物 | Trimethylamine oxide | HCID 1145 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Bis(1,2-dimethylpropyl)borane | HCID 192733 | — |
| 反応物 | Trimethyl[(oct-1-yn-4-yl)oxy]silane | HCID 12786181 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1-Iodo-4-trimethylsiloxy-trans-1-octene | HCID 12851277 | — |
反応手順
To a stirred solution of 0.020 moles of freshly prepared bis-(3-methyl-2-butyl)borane in 300 ml of tetrahydrofuran at 0°-5° C is added dropwise a solution of 19.8 g of 4-trimethylsiloxy-1-octyne in 30 ml of tetrahydrofuran. The resulting mixture is stirred at ambient temperature for several hours, cooled in an ice bath, and treated with 53 g of trimethylamine oxide. The mixture is stirred several hours at 25°-40° C and then poured into 2 liters of 15% sodium hydroxide. The resulting mixture is treated immediately with a solution of 140 g of iodine in 300 ml of tetrahydrofuran. After 0.5 hour the organic phase is separated and the aqueous phase is extracted with ether. The combined organic layers are washed with water, sodium thiosulfate solution, and brine; dried over magnesium sulfate; and concentrated to give an oil, pmr spectrum (CDCl 3): 6.2 (d, ICH=) and 6.7 (quintuplet, =C-).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04131737 |
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| 出典データセット | uspto-grants-1978_12 |
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| ORD ID | ord-ee8814a93a8044e3904426eff2a6053d |
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| 出典メモ | uspto-grants-1978_12 |
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