関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1,5-Dimethyltetrazole | HCID 78825 | — |
| 反応物 | Bis(2,4-dimethylphenyl)methanone | HCID 12274022 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1,1-Bis(2,4-dimethylphenyl)-2-(1-methyl-1H-tetrazol-5-yl)ethanol | HCID 14723946 | 86% |
反応手順
A solution of 1,5-dimethyltetrazol (8.9 g, 91.0 mmoles) in 100 mL of dry tetrahydrofuran at -60° C. was treated with n-butyl lithium (48 mL of 1.89M solution, 91.0 mmoles). After stirring for 20 minutes, 2,2',4,4'-tetramethylbenzophenone (18 g, 76 mmoles) [prepared by the procedure described in J. Am. Chem. Soc., 81, 4858 (1959)] in 50 mL dry tetrahydrofuran was added and the solution was stirred for 1 hour during which time it was allowed to warm to -20° C. The reaction was quenched with 1N HCl, then extracted with chloroform. The combined organic extracts were dried (MgSO4) and evaporated to give 22 g of the title compound; m.p.=175°-177° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05068346 |
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| 出典データセット | uspto-grants-1991_11 |
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| ORD ID | ord-993db651a548428c82b5a92be3b7db66 |
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| 出典メモ | uspto-grants-1991_11 |
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