HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608832Generated: November 1, 2026
N-(3-Bromopropyl)-2-nitrobenzamide → HCID 54510921, compound
https://huagongshe.com/reaction/1608832
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-(3-Bromopropyl)-2-nitrobenzamide | HCID 20085691 | — |
| Reactant | HCID 178418441 | HCID 178418441 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54510921 | HCID 54510921 | 18.2% |
Reaction Steps
A solution of 24.5 g (0.085 mol) of N-(3-bromopropyl)-2-nitrobenzamide in 75 ml of dimethylformamide was slowly added to a solution of 7.00 g (0.10 mol) of tetrazole. The resulting solution was heated to 50° C. and allowed to react overnight. When the reaction was complete, as determined by thin layer chromatography, most of the dimethylformamide was removed under reduced pressure. The resultant residue was diluted with water, causing a precipitate to form. The precipitate was isolated by filtration and dried under vacuum. Thin layer chromatography and nuclear magnetic resonance spectroscopy indicated the presence of two isomers; namely, the N-1 and N-2 alkylated tetrazoles (75:25 ). The N-2 alkylated compound was isolated by column chromatography to provide 4.3 g of the desired subtitled intermediate. The N-1 alkylated compound was isolated by twice crystallizing the precipitate from cyanomethane to provide 3.72 g of that compound. (m.p. 148°-150° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05397798 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-6f00463f05e746d698995d339331fe6f |
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| Source note | uspto-grants-1995_03 |
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