HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330656Generated: October 25, 2026
1,5-Dimethyltetrazole → 1,1-Bis(2,4-dimethylphenyl)-2-(1-methyl-1H-tetrazol-5-yl)ethanol
https://huagongshe.com/reaction/330656
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,5-Dimethyltetrazole | HCID 78825 | — |
| Reactant | Bis(2,4-dimethylphenyl)methanone | HCID 12274022 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,1-Bis(2,4-dimethylphenyl)-2-(1-methyl-1H-tetrazol-5-yl)ethanol | HCID 14723946 | 86% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04897490 |
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| Source dataset | uspto-grants-1990_01 |
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| ORD ID | ord-22fb5a3719654704a79e5fde0824a246 |
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| Source note | uspto-grants-1990_01 |
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