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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289017Generated: October 29, 2026

Hydrochloric Acid → Pentoxazone

https://huagongshe.com/reaction/2289017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
Reactant3-Butenoic acid, 2-hydroxy-3-methyl-, ethyl esterHCID 10855589—
ReactantN-[4-Chloro-5-(cyclopentyloxy)-2-fluorophenyl]carbamic acid ethyl esterHCID 11033971—
CatalystTetrabutylammonium ChlorideHCID 70681—
ProductPentoxazoneHCID 1171423436.7%

Reaction Conditions

Temperature75 °C

Reaction Steps

Ethyl N-(4-chloro-5-cyclopentyloxy-2-fluorophenyl)carbamate (3.01 g, 10 mmol), ethyl 2-hydroxy-3-methyl-3-butenoate (2.16 g, 15 mmol) and tetrabutylammonium chloride (278 mg, 1.0 mmol) were introduced into a flask (25 cc) equipped with a distillation unit, and the reaction was conducted at 200° C. for 1.5 hours. After completion of the reaction, the reaction solution was allowed to cool to 70 to 80° C., and a mixed solution consisting of methanol (5 mL) and 6N hydrochloric acid (0.25 mL) was added thereto and mixed homogeneously. Then, the reaction solution was left to stand at room temperature. The precipitated solid was collected by filtration, washed with a mixed solution consisting of methanol (8 mL) and 6N hydrochloric acid (0.4 mL) and then water (10 mL) and dried completely under reduced pressure to obtain 3-(4-chloro-5-cyclopentyloxy-2-fluorophenyl)-5-isopropylidene-1,3-oxazolidine-2,4-dione (1.30 9, yield 36.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090946
Source datasetuspto-grants-2000_07
ORD IDord-8f4794e82eff4ba790cd525a3b3ca7aa
Source noteuspto-grants-2000_07