関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1-Pentyne | HCID 12309 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Propanal, 3-chloro- | HCID 29596 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 生成物 | 1-Chlorooct-4-yn-3-ol | HCID 20465548 | — |
反応手順
To 68 ml. of 1.6 M butyllithium in hexane at -50° C. is added dropwise, with stirring, 7.4 g. of 1-pentyne. The resulting white sludge is diluted with 20 ml. of hexane, brought to 10° C. and treated with 11 g. of freshly prepared β-chloropropionaldehyde (Org. Syn., Coll. Vol. I, p. 166) at such a rate that the temperature is maintained at 10°-15° C. The solution is allowed to stir at ambient temperature for 18 hours then treated with saturated ammonium chloride solution. The organic phase is separated, washed with dilute hydrochloric solution, dried with anhydrous magnesium sulfate and taken to dryness. Distillation gives 5.1 g. of product b.p. 65°-66° C. at 0.3 nm.; λmax. 2.95 (--OH) and 4.55μ (--C≡C--); vapor phase chromatography shows one peak.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04343949 |
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| 出典データセット | uspto-grants-1982_08 |
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| ORD ID | ord-468d1b6d25904b579ad5f074478fc524 |
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| 出典メモ | uspto-grants-1982_08 |
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