Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Cyclopentyloxy-4-methoxybenzaldehydeHCID 2735893—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 178509273HCID 178509273—
SolventMethanolHCID 887—
ProductHCID 178491044HCID 17849104449%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05922751
Source datasetuspto-grants-1999_07
ORD IDord-79ab203ca4b641d487ace948b8e80f72
Source noteuspto-grants-1999_07