Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519692Generated: November 2, 2026

Ethanol → HCID 71268205, compound

https://huagongshe.com/reaction/1519692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium HydroxideHCID 14797—
ReactantPotassium bisulfateHCID 516920—
ReactantHCID 71268190HCID 71268190—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 71268205HCID 71268205104.6%

Reaction Steps

A 0.84 mol/L potassium hydroxide aqueous solution (3.0 mL) was added to an ethanol (3.0 mL)-THF (3.0 mL) solution of 4-{[1-ethoxy-2-methyl-3-(methylamino)-1,3-dioxopropan-2-yl](methyl)carbamoyl}biphenyl (0.30 g) as obtained in Example 12-(1), and the mixture was stirred for 4.5 hours at room temperature. Under ice cooling, water and a 2.0 mol/L potassium hydrogen sulfate aqueous solution were added to adjust the mixture to pH 7, followed by extracting the mixture with chloroform. The organic layer was dried over anhydrous magnesium sulfate, and then the desiccant was filtered out. The solvent was distilled off under reduced pressure to obtain 4-{[2-carboxy-1-(methylamino)-1-oxopropan-2-yl](methyl)carbamoyl}biphenyl (orange solid) (0.29 g, 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073821B2
Source datasetuspto-grants-2015_07
ORD IDord-fae2df811a0944cbb921891e45880b98
Source noteuspto-grants-2015_07