HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225418Generated: October 30, 2026
Hydrochloric Acid → N-allyloxy-3,5-dichloro-1-methylpyrazole-4-carboxylic acid amide
https://huagongshe.com/reaction/225418
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,5-Dichloro-1-methylpyrazole-4-carbohydroxamic acid | HCID 57752427 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-allyloxy-3,5-dichloro-1-methylpyrazole-4-carboxylic acid amide | HCID 57752428 | 72.2% |
Reaction Steps
In a solution of potassium carbonate (15.8 g, 114 mmol) in water (60 ml), a solution of 3,5-dichloro-1-methylpyrazole-4-carbohydroxamic acid (20.0 g, 95.2 mmol) and allyl bromide (13.8 g, 114 mmol) in toluene (60 ml) was added, and stirred at 50° C. for 3 hours. After cooling to room temperature, the mixture was adjusted to pH 1 by adding 35% hydrochloric acid, precipitated solid was filtered off, washed with water and toluene in that order, and dried to obtain the aimed product (17.2 g). Melting point 96-97° C. Proton nuclear magnetic resonance chemical shift values δ (ppm) (in CDCl3) 3.84 (s, 3H), 4.51 (d, J=6.3 Hz, 2H), 5.3-5.46 (m, 2H), 5.94-6.13 (m, 1H), 8.80 (brs, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07557067B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-88d79534543f45ca8f26511391ec5734 |
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| Source note | uspto-grants-2009_07 |
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