Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2057344Generated: October 27, 2026

Ethyl Acetate → HCID 178471716, compound

https://huagongshe.com/reaction/2057344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantHCID 178468267HCID 178468267—
SolventWaterHCID 962—
ProductHCID 178471716HCID 17847171689%

Reaction Conditions

Temperature100 °C

Reaction Steps

400 mg (0.89 mmol) trans-4-{4-[Methyl-(4-trifluoromethyl-benzenesulfonyl)-amino]-cyclohexyloxy}-butyrimidic acid ethyl ester were suspended in 10 ml water and heated to 100° C. for 2.5 h. EtOAc was added, and the inorganic phase was extracted with EtOAc. The combined organic phases were dried over Na2SO4 and evaporated to give 355 mg (89%) trans-4-{4-[Methyl-(4-trifluoromethyl-benzenesulfonyl)-amino]-cyclohexyloxy}-butyric acid ethyl ester as yellow oil, MS: 452 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07335687B2
Source datasetuspto-grants-2008_02
ORD IDord-8762e8a9462543b3ba7d0643fdd1663d
Source noteuspto-grants-2008_02