関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hexanal | HCID 6184 | — |
| 反応物 | 1,3-Butadiene | HCID 7845 | — |
| 反応物 | 1-Butyne | HCID 7846 | — |
| 反応物 | Dimethylacetylene | HCID 10419 | — |
| 反応物 | 1,2-Butadiene | HCID 11535 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 3-Decyn-5-ol | HCID 21518441 | — |
反応手順
Following the procedure of Example 1, but with a pressure equalizing dropping funnel in place of the gas addition tube, 5.2 g. of lithium metal powder and 125 ml. of tetrahydrofuran are added to the flask. 65 g. of ammonia gas is condensed into the slurry with stirring forming a liquid-copper-gold colored lithium ammonia adduct. 190 g. of a mixture containing about 18% 1,2-butadiene, 21% 1,3-butadiene, 4% 1-butyne, 3.3% 2-butyne and about 25% isomeric butenes dissolved in 800 ml. tetrahydrofuran was added over a 70 minute period with stirring while maintaining the temperature at about 50°C. to 60°C. The mixture was refluxed to drive off excess gases and cooled. An aliquot of the product was reacted with 1-hexanal producing 3-decyn-5-ol which by gas chromotograph analysis, establishes a yield of butynyllithium in excess of 90%, based on lithium.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US03975453 |
|---|
| 出典データセット | uspto-grants-1976_08 |
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| ORD ID | ord-a28dd0458317429e893d593529ac2648 |
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| 出典メモ | uspto-grants-1976_08 |
|---|