関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1,5-Dimethyltetrazole | HCID 78825 | — |
| 反応物 | 2,2'-Difluoro-4,4'-dimethylbenzophenone | HCID 14723981 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1,1-Bis(2-fluoro-4-methylphenyl)-2-(1-methyl-1H-tetrazol-5-yl)ethanol | HCID 14723992 | — |
反応手順
To a solution of 1,5-dimethyltetrazole (4.6 g, 4.7 mmoles) in tetrahydrofuran (40 mL) at -50° C. was added butyl lithium solution (21.4 mL of a 2.2 M solution, 4.7 mmoles). After stirring for 10 minutes, a solution of 2,2'-difluoro-4,4'-dimethylbenzophenone in tetrahydrofuran (15 mL) was added. The solution was stirred for 2.5 hours during which time it was allowed to warm to -10° C. The reaction was quenched by adding 1N hydrochloric acid. The layers were separated and the aqueous layer was extracted with methylene chloride. The combined organic fractions were dried (MgSO4) and evaporated. The residue was triturated with diethyl ether and crystallized from isopropyl acetate to give 8.0 g of the title compound; m.p=150°-151° C. MS: M+ =344.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04939265 |
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| 出典データセット | uspto-grants-1990_07 |
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| ORD ID | ord-c55c45413b0d41ac9260d7a68c037e16 |
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| 出典メモ | uspto-grants-1990_07 |
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