참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,5-Dimethyltetrazole | HCID 78825 | — |
| 반응물 | Bis(2,4-dimethylphenyl)methanone | HCID 12274022 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1,1-Bis(2,4-dimethylphenyl)-2-(1-methyl-1H-tetrazol-5-yl)ethanol | HCID 14723946 | 86% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04897490 |
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| 출처 데이터셋 | uspto-grants-1990_01 |
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| ORD ID | ord-22fb5a3719654704a79e5fde0824a246 |
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| 출처 메모 | uspto-grants-1990_01 |
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