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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1849803Generated: November 1, 2026

Hydrochloric Acid → 5-Chloro-2-fluoro-4-((4-oxocyclohexyl)oxy)benzoic acid

https://huagongshe.com/reaction/1849803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-(1,4-Dioxaspiro[4.5]decan-8-yloxy)-5-chloro-2-fluorobenzoic acidHCID 86703685—
SolventAcetoneHCID 180—
SolventSodium chloride; waterHCID 57417360—
Product5-Chloro-2-fluoro-4-((4-oxocyclohexyl)oxy)benzoic acidHCID 8670368645%

Reaction Steps

To a solution of 4-(1,4-dioxaspiro[4.5]decan-8-yloxy)-5-chloro-2-fluorobenzoic acid (2.95 g, 8.92 mmol) in acetone (100 mL) was added 3 M hydrochloric acid (80 mL). The solution was heated to reflux for 17 hours and cooled to ambient temperature. The mixture was diluted with brine (200 mL) and extracted with ethyl acetate (3×150 mL). The combined organic layers were dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo to dryness. The residue was purified by column chromatography with a gradient of a solution of 0.2% acetic acid in ethyl acetate and hexanes from 0-50% to afford the title compound as a colorless solid (1.14 g, 45%): 1H NMR (300 MHz, CDCl3) δ 8.07 (d, J=7.6 Hz, 1H), 6.77 (d, J=11.9 Hz, 1H), 4.82 (br s, 1H), 2.81-2.70 (m, 2H), 2.41-2.35 (m, 4H), 2.15-2.03 (m, 2H) (OH not observed); MS (ES−) m/z 285.1, 287.1 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952169B2
Source datasetuspto-grants-2015_02
ORD IDord-897044bf85b346299e4bd12275263784
Source noteuspto-grants-2015_02