HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614554Generated: October 30, 2026
Water → N-{[dimethyl-(4-fluorobenzyl)silyl]methyl}-1,2,4-triazole hydrochloride
https://huagongshe.com/reaction/1614554
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1H-1,2,4-Triazole | HCID 9257 | — |
| Reactant | Chloromethyl-dimethyl(4-fluorobenzyl)silane | HCID 15338764 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | N-{[dimethyl-(4-fluorobenzyl)silyl]methyl}-1,2,4-triazole hydrochloride | HCID 19007220 | — |
Reaction Steps
After adding 10 g of 1,2,4-triazole to 10.8 g of chloromethyl-dimethyl-(4-fluorobenzyl)silane dissolved in 50 ml of xylene, the reaction mixture is refluxed for 8 hours, then 200 ml of water are added and the phases are separated. The organic phase is washed 3 times with a total of 150 ml of water, dried over anhydrous magnesium sulfate and after filtration the filtrate is evaporated to solvent-free. The pale yellow oily residue is dissolved in 70 ml of methyl propyl ketone, the solution is acidified to pH 4.5 by adding methanolic hydrogen chloride solution and then concentrated to a volume of 40 ml by distillation under atmospheric pressure. The crystals precipitated are filtered at 0° C. to give the named product in a yield of 6.56 g (46%), m.p.: 113°-114° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05198446 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-617a74698fd643bdad6eaf97cdf278db |
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| Source note | uspto-grants-1993_03 |
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