HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360412Generated: October 30, 2026
Ammonium Hydroxide → HCID 66958785, compound
https://huagongshe.com/reaction/1360412
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 66958280 | HCID 66958280 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 66958785 | HCID 66958785 | — |
Reaction Steps
A solution of ethyl 1-benzyl-5-(2-methylpropyl)-1H-pyrazole-3-carboxylate (30 g) in methanol (60 mL) was treated with ammonium hydroxide (60 mL) according to a modification of the method described in Part D of Examples 1-4. The reaction was heated for 14 hours. At the end of the reaction, the methanol was removed under reduced pressure, and the remaining solution was extracted with tert-butyl methyl ether (3×). The combined extracts were dried over magnesium sulfate, filtered, and concentrated under reduced pressure. Toluene was added twice and removed under reduced pressure to remove residual water. Hexane was added to the residue; crystals formed and were isolated by filtration, washed with hexane, and air-dried overnight to provide 6.93 g of 1-benzyl-5-(2-methylpropyl)-1H-pyrazole-3-carboxamide as small, off-white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07879849B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-4654c9d4b6204d73af4369e1751eaa9f |
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| Source note | uspto-grants-2011_02 |
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