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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289014Generated: October 29, 2026

Hydrochloric Acid → Pentoxazone

https://huagongshe.com/reaction/2289014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
Reactant3-Butenoic acid, 2-hydroxy-3-methyl-, ethyl esterHCID 10855589—
Reactantmethyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamateHCID 15766845—
CatalystTributylamineHCID 7622—
ProductPentoxazoneHCID 1171423454.5%

Reaction Conditions

Temperature75 °C

Reaction Steps

Methyl N-(4-chloro-5-cyclopentyloxy-2-fluorophenyl)carbamate (2.87 g, 10 mmol), ethyl 2-hydroxy-3-methyl-3-butenoate (4.32 g, 30 mmol), ferric chloride (162 mg, 1.0 mmol) and tributylamine (92.7 mg, 0.5 mmol) were introduced into a flask (25 cc) equipped with a distillation unit, and the reaction was conducted at 200° C. for 3 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 (0.8 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 (1.93 g, yield 54.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090946
Source datasetuspto-grants-2000_07
ORD IDord-ab997b7e954d4dacbfb0abb4b4861f3f
Source noteuspto-grants-2000_07