HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582125Generated: October 25, 2026
3-Cyclopentyloxy-4-methoxybenzaldehyde → HCID 178491044, compound
https://huagongshe.com/reaction/582125
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 | 48.7% |
Reaction Steps
A suspension of 3-amino-4-pyrazole carboxylic acid (3.56 g, 28 mmol) in 400 ml of methanol and 3-cyclopentyloxy-4-methoxybenzaldehyde (5.06 g, 23 mmol) was stirred at room temperature for 16 hours with sodium cyanoborohydride, 1.85 g (95% pure, 28 mmol). The methanol was evaporated under reduced pressure and the residue was taken up in 100 ml of 15% sodium hydroxide and extracted twice with 100 ml portions of ether. The aqueous layer was acidified to pH 5 with 5N hydrochloric acid and extracted twice with 100 ml portions of ethyl acetate. The ethyl acetate was dried over sodium sulfate and evaporated. The residue was triturated with ether to give 3.7 g of 3-(3-cyclopentyloxy-4-methoxybenzylamino)-4-pyrazolecarboxylic acid (48.7%). Pure 3-(3-cyclopentyloxy-4-methoxybenzylamino)pyrazole carboxylic acid shows mp. 134-136° C. after crystallization 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-f8bef5900ac64aaf8c3cb9782a42a350 |
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| Source note | uspto-grants-1999_07 |
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