Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 21833670 | HCID 21833670 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178418936 | HCID 178418936 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53869820 | HCID 53869820 | — |
Reaction Steps
A mixture of 2.26 g of 2H- 1,2,3-triazole, 1.31 g of sodium hydride (60% oil dispersion) and 100 ml of anhydrous N,N-dimethylformamide was stirred at 60° to 70° C. under a nitrogen atmosphere for 2 hours. After the evolution of hydrogen gas ceased, the mixture was cooled to 10° C. To this mixture was added dropwise an anhydrous N,N-dimethylformamide (150 ml) solution of 10 g of 4-bromomethyl-2-chlorophenyl 2,2-dimethylpropanoate at room temperature under stirring over 1 hour, and the mixture was stirred at 80° C. for 1 hour. After cooling, the reaction mixture was poured into ice water, which was extracted with ethyl acetate. The organic layer was washed with saturated aqueous ammonium chloride solution and then saturated sodium chloride solution, dried with anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography, which afforded 2-chloro-4-(2-2H-1,2,3-triazolyl)methylphenyl 2,2-dimethylpropanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05972949 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-1d7e7f6dccec4fdfa8ddc7f9c5ba96b3 |
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| Source note | uspto-grants-1999_10 |
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