Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Triethyl phosphite | HCID 31215 | — |
| Reactant | HCID 23465185 | HCID 23465185 | — |
| Product | HCID 23465188 | HCID 23465188 | — |
Reaction Steps
155.6 g of 2-(p-bromomethyl-phenyl)-4-methyl-5-carboethoxy-2H-1,2,3-triazole in 430 ml of triethyl phosphite are heated to 150° C. in the course of 21/2 hours and the mixture is kept at this temperature for 3 hours, with stirring, ethyl bromide distilling off. The reaction mixture is evaporated under a waterpump vacuum. The residual dark viscous oil is dissolved in 300 ml of methylene chloride and, after the addition of bleaching earth, the solution is filtered to give a clear filtrate and 300 ml of hexane are added to the filtrate. The resulting mixture is then concentrated to 200 ml and cooled to 0° to 5° C. and the product which has crystallised out is filtered off with suction and dried in vacuo. This gives 56.6 g of 2-(p-diethylphosphonomethyl-phenyl)-4-methyl-5-carboethoxy-2H-1,2,3-triazole of the formula ##STR59##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04261855 |
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| Source dataset | uspto-grants-1981_04 |
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| ORD ID | ord-3e5325530b584e88ac5af723a76723ad |
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| Source note | uspto-grants-1981_04 |
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