HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628497Generated: October 29, 2026
Dimethylformamide → 1-(2-Methyl-3-bromophenyl)-4-methyl-1,4-dihydrotetrazol-5-one
https://huagongshe.com/reaction/628497
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(2-Methyl-3-bromophenyl)-1,4-dihydrotetrazol-5-one | HCID 136646186 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(2-Methyl-3-bromophenyl)-4-methyl-1,4-dihydrotetrazol-5-one | HCID 89875845 | — |
Reaction Steps
To a mixture of 1-(2-methyl-3-bromophenyl)-1,4-dihydrotetrazole-5-one (described in Reference Preparation example 9) 31.40 g and N,N-dimethylformamide 250 ml was added 60% sodium hydride 5.90 g under ice-cooling. The reaction mixture was raised to room temperature and was stirred for one hour. To the reaction mixture was added methyl iodide 8.4 ml under ice-cooling. The resulting mixture was raised to room temperature and was stirred for fourteen hours. To the reaction mixture was added water and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with 10% hydrochloric acid, water and saturated saline, and was dried over anhydrous magnesium sulfate and was then concentrated under reduced pressure. The resulting residue was subjected to a silica gel column chromatography to give 1-(2-methyl-3-bromophenyl)-4-methyl-1,4-dihydrotetrazole-5-one 8.47 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09314023B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-cc6b3a3578ee4d12aef6e7c57a2680f8 |
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| Source note | uspto-grants-2016_04 |
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