Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1H-1,2,3-Triazole | HCID 67516 | — |
| Reactant | HCID 21833670 | HCID 21833670 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Product | HCID 70150069 | HCID 70150069 | — |
Reaction Steps
A mixture of 2H-1,2,3-triazole (2.26 g), sodium hydride (60%, 1.31 g) and anhydrous N,N-dimethylformamide (100 ml) 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 4-bromomethyl-2-chlorophenyl 2,2-dimethylpropanoate (10 g) 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 | US05684022 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-964015d45a8b46b1ab4ef83c728c1796 |
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| Source note | uspto-grants-1997_11 |
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