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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870360Generated: October 30, 2026

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

https://huagongshe.com/reaction/1870360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium CarbonateHCID 10340—
Reactant3-Cyclopentyloxy-4-methoxybenzaldehydeHCID 2735893—
ReactantSodium BisulfiteHCID 23665763—
SolventPotassium PermanganateHCID 516875—
Product3-(Cyclopentyloxy)-4-methoxybenzoic acidHCID 2779323—

Reaction Conditions

Temperature50 °C

Reaction Steps

A stirred saturated aqueous solution of potassium permanganate (100 mL) is treated with 3-cyclopentyloxy-4-methoxybenzaldehyde (7.4 g; that is prepared as described hereinbefore in Reference Example 1) and sodium carbonate (3.4 g) and the mixture is stirred at 50° C. for 1 hour, and then cooled to room temperature. The reaction mixture is acidified by treatment with concentrated hydrochloric acid and then it is treated with aqueous sodium bisulfite solution until a colorless solution is obtained. The reaction mixture is extracted with dichloromethane (2×100 mL) and the organic extracts are dried over magnesium sulfate and concentrated. The resulting residue is recrystallized from diethyl ether, to give 3-cyclopentyloxy-4-methoxybenzoic acid (4.78 g) in the form of white crystals. [NMR(CDCl3): 1.7(s,2H),1.8-2.2 (m,6H),3.95(s,3H),4.85(s,1H),6.9(bs,1H)7.6(bs,1H), 7.8(s,1H),9.8(s,1H); Elemental analysis: C,65.6; H,6.8%; Calculated: C,66.1; H,6.8%].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06096768
Source datasetuspto-grants-2000_08
ORD IDord-efb5755b7f214886afda5650f331cb53
Source noteuspto-grants-2000_08