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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 617229Generated: October 29, 2026

Hydrochloric Acid → Famoxadone

https://huagongshe.com/reaction/617229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhenylhydrazineHCID 7516—
ReactantDiphenyl EtherHCID 7583—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantEthyl 2-(4-phenoxyphenyl)lactateHCID 10859095—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductFamoxadoneHCID 21303281.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of 14.3 g of ethyl 2-(4-phenoxyphenyl)lactate (34 g of a mixture containing 14.3 g of ethyl 2-(4-phenoxyphenyl)lactate and 19.7 g of diphenyl ether), 9.7 g of 1,1'-carbonyldiimidazole and 100 mL of methylene chloride was agitated at 25° C. for 19 h. Water (0.30 mL) was added and the mixture was agitated for 15 min. Then, 5 mL of acetic acid and 7.4 g of phenylhydrazine were added. After agitating at 25° C. for 24 h, 100 mL of water was added. The pH was lowered to 2 with hydrochloric acid, and the aqueous layer was removed. After washing the methylene chloride layer with 50 mL of water, the solvent was evaporated under vacuum. The oily residue was mixed with 150 mL hexane and 15 mL of ethyl acetate, heated to 65° C., cooled to 20° C., and then filtered. The solids were washed with 100 mL of a mixture of 20 mL ethyl acetate and 80 mL of hexane and then dried. The title product (15.2 g) was obtained with a m.p. of 137-139° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05948805
Source datasetuspto-grants-1999_09
ORD IDord-b83e4c66d9074dc2bbdf9624599571f2
Source noteuspto-grants-1999_09