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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871527Generated: November 3, 2026

3-Cyclopentyloxy-4-methoxybenzaldehyde → HCID 178490969, compound

https://huagongshe.com/reaction/1871527

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Cyclopentyloxy-4-methoxybenzaldehydeHCID 2735893—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 178508070HCID 178508070—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
ProductHCID 178490969HCID 17849096934%

Reaction Steps

To a stirred solution of 5-amino-1,2,3-triazole (3.0 g, 0.036 mol) in 100 ml of methanol and 15 ml of 1 N HCl was added sodium cyanoborohydride (1.89 g, 0.030 mol) and 3-cyclopentyloxy-4-methoxybenzaldehyde (6.6 g, 0.30 mol). The reaction mixture was stirred at room temperature for 64 hours and then acidified to pH 2 with concentrated HCl. The solution was evaporated at reduced pressure and the residue was treated with water (100 ml) and extracted twice with 100 ml portions of ethyl acetate. The ethyl acetate extracts were combined and extracted twice with 50 ml portions of 3N HCl and then discarded. The aqueous extracts were combined with the original aqueous layer and basified to pH 12 with potassium hydroxide pellets. The alkaline solution was extracted twice with 100 ml portions of ethyl acetate. The ethyl acetate extracts were combined and evaporated to give a solid which was crystallized from ethyl acetate to give 2.9 g (34%) of the title compound mp 113-114° C. collected in two crops.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06103749
Source datasetuspto-grants-2000_08
ORD IDord-c45a6bcee590461d8625cefc0d8d38d8
Source noteuspto-grants-2000_08