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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871525Generated: November 3, 2026

3-Cyclopentyloxy-4-methoxybenzaldehyde → HCID 178491044, compound

https://huagongshe.com/reaction/1871525

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Cyclopentyloxy-4-methoxybenzaldehydeHCID 2735893—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 178509273HCID 178509273—
SolventMethanolHCID 887—
ProductHCID 178491044HCID 17849104448.7%

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 5 N 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06103749
Source datasetuspto-grants-2000_08
ORD IDord-5a3ba926bb8549af95d78d6dab394303
Source noteuspto-grants-2000_08