HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181149Generated: October 26, 2026
3-Bromo-1-propanol → 3-(3,5-Dibromo-4-nitropyrazol-1-yl)propan-1-ol
https://huagongshe.com/reaction/1181149
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Bromo-1-propanol | HCID 12308 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3,5-Dibromo-4-nitro-1H-pyrazole | HCID 13707994 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(3,5-Dibromo-4-nitropyrazol-1-yl)propan-1-ol | HCID 23104170 | 80.3% |
Reaction Steps
A mixture of 3,5-dibromo-4-nitropyrazole (2) (2.0 g; 7.38 mmol) in DMF (9.5 ml) was added over 15 minutes to a suspension of NaH (0.32 g, 8.0 mmol; 60% dispersion in oil, prewashed with hexane) in DMF (16 ml) with stirring and under an inert atmosphere. After stirring for 15 minutes, a solution of 3-bromo-1-propanol (1.0 g; 7.19 mmol) in DMF (3.2 ml) was added dropwise. The reaction mixture was heated at 80° C. for 2 hours (monitored by TLC) and the DMF was then evaporated off under reduced pressure. A mixture of DCM/water (20 ml, 1/1) was added. The organic phase was dried over Na2SO4 and the solvent was evaporated off under reduced pressure. The crude reaction product was obtained as a black oil (1.9 g, 79%), which was used without further purification in the amination step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07285136B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-8aa8bdc7fe944f4a808d967c3a9b2595 |
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| Source note | uspto-grants-2007_10 |
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