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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599380Generated: October 26, 2026

Acetic Acid → HCID 22672522, compound

https://huagongshe.com/reaction/599380

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPotassium HydroxideHCID 14797—
ReactantEthyl 4-((4-((2-chloro-4-nitrophenyl)diazenyl)phenyl)(3-hydroxypropyl)amino)butanoateHCID 22672523—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22672522HCID 22672522—

Reaction Conditions

Temperature4 °C

Reaction Steps

To a stirred solution of 20 (4.48 g, 10 mmole) in 40 mL of THF added 40 mL of ethanol followed by a solution of KOH (0.84 g,15 mmol) in 20 mL of water and 20 mL of ethanol. The mixture is stirred overnight and concentrated. The residue suspended in 125 mL of water, treated with 2.6 mL (˜3 eqv.) of acetic acid, and cooled to 4° C. The resulting solid is filtered off, washed with water, and dried. Yield is quantitative. 1H NMR (DMSO-d6) δ 8.42 (d, J=2.5 Hz, aromatic proton, 1H), 8.23 (dd, J1=9 Hz, J2=2.5 Hz, aromatic proton, 1H), 7.82 (d, J=9 Hz, 2H), 7.90 (d, J=9Hz, 1H), 7.03 (d, J=9 Hz, aromatic protons, 2H), 4.8 (br s, OH, 1H), 3.5 (m, aliphatic protons, 6H), 1.86 (t, J=6 Hz, aliphatic protons, 2H), 1.72 (m, aliphatic protons, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897736B2
Source datasetuspto-grants-2011_03
ORD IDord-836107a7fb5d4b70a7f61c16fb9a81b5
Source noteuspto-grants-2011_03