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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250850Generated: November 4, 2026

Hydrochloric Acid → 3-(Cyclopentyloxy)-4-methoxybenzoic acid

https://huagongshe.com/reaction/1250850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium PermanganateHCID 516875—
Reactant3-Cyclopentyloxy-4-methoxybenzaldehydeHCID 2735893—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
Product3-(Cyclopentyloxy)-4-methoxybenzoic acidHCID 277932367%

Reaction Steps

A solution of tetrabutylammonium bromide (111.68 g, 0.336 moles) in water (400 ml) was added under stirring to a solution of potassium permanganate (53.1 g, 0.336 moles) in water (1 l). The obtained solid was separated by filtration, washed with water and dissolved in 500 ml of pyridine. This solution was dropped into one of crude 3-cyclopentyloxy-4-methoxy benzaldehyde (obtained as described in J. Med. Chem., 1995, 38, page 4851) (74 g, 0.336 moles) in pyridine (200 ml), under stirring in water/ice. At the end 3 l of ice were added and it was acidified by dropping 850 ml of 12N HCl. The stirring was kept for further 1.5 hours, then the solid was separated by filtration and extracted under stirring for 30 minutes with ethyl acetate (2 l). The residual solid was removed and the mother liquors were further extracted with ethyl acetate (2×700 ml). The organic phases were washed with water, dried on sodium sulphate and concentrated to small volume to give 53.2 g of the title compound (yield: 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340684B1
Source datasetuspto-grants-2002_01
ORD IDord-266a1c8a7f7d4ff6b8c2320bcdde221d
Source noteuspto-grants-2002_01