Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289013Generated: October 27, 2026

Hydrochloric Acid → Pentoxazone

https://huagongshe.com/reaction/2289013

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—
CatalystTributylamineHCID 7622—
ProductPentoxazoneHCID 1171423467.4%

Reaction Conditions

Temperature200 °C

Reaction Steps

Ethyl N-(4-chloro-5-cyclopentyloxy-2-fluorophenyl)carbamate (6.02 g, 20 mmol), ferric chloride (53.5 mg, 0.33 mmol) and tributylamine (185 mg, 1.00 -mmol) were introduced into a two-necked flask (50 cc) equipped with a distillation unit and heated to 200° C. Ethyl 2-hydroxy-3-methyl-3-butenoate (4.33 g, 30 mmol) was added dropwise to the mixed solution over 30 minutes, and after the addition, the solution was stirred at 200° C. for 3.5 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 (10 mL) and 6N hydrochloric acid (0.5 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 (20 mL) and 6N hydrochloric acid (1 mL) and then water (20 mL) and dried completely under reduced pressure to obtain 3-(4-chloro-5-cyclopentyloxy-2-fluorophenyl)-5-isopropylidene-1,3-oxazolidine-2,4-dione (4.77 g, yield 67.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090946
Source datasetuspto-grants-2000_07
ORD IDord-4fec8aff4b59401382fd0f7e77ef75ea
Source noteuspto-grants-2000_07