HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582130Generated: October 25, 2026
3-Cyclopentyloxy-4-methoxybenzaldehyde → HCID 178491044, compound
https://huagongshe.com/reaction/582130
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Cyclopentyloxy-4-methoxybenzaldehyde | HCID 2735893 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 178509273 | HCID 178509273 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178491044 | HCID 178491044 | 49% |
Reaction Steps
To a suspension of 3-aminopyrazole-4-carboxylic acid (3.56 g, 0.023 mol) in 400 ml of methanol was added 3-cyclopentyloxy-4-methoxybenzaldehyde (5.06 g, 0.023 mole) and 95% sodium cyanoborohydride (1.85 g, 0.028 mol). The reaction mixture was stirred for 16 hours and then the methanol was evaporated under reduced pressure. The residue was treated with 100 ml of 15% aqueous NaOH and extracted twice with 100 ml portions of ether. The aqueous layer was acidified to pH 5 with 5N aqueous HCl and extracted twice with 100 ml portions of ethyl acetate. The ethyl acetate extracts were evaporated under reduced pressure and the residue was triturated with ether to give 3.7 g (49%) of the title compound, mp 134-136°, after recrystallization from methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05922751 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-79ab203ca4b641d487ace948b8e80f72 |
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| Source note | uspto-grants-1999_07 |
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