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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544954Generated: November 3, 2026

Glycolic Acid → HCID 57550365, compound

https://huagongshe.com/reaction/544954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycolic AcidHCID 757—
ReactantTriethylamineHCID 8471—
Reactant1-(2,4-dichlorophenyl)piperazine DihydrochlorideHCID 2737526—
ReactantHCID 178418300HCID 178418300—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 57550365HCID 5755036545.2%

Reaction Steps

To a screw-cap vial was added glycolic acid (100 mg, 1.31 mmol), 1-(3-dimthylaminopropyl)-3-ethylcarbodiimide hydrochloride (277.3 mg, 1.45 mmol), hydroxybenzotriazole (195.5 mg, 1.45 mmol), 1-(2,4-dichlorophenyl)-piperazine dihydrochloride (439.8 mg, 1.45 mmol), triethylamine (0.55 mL, 3.94 mmol) and N,N-dimethylformamide (5 mL). The resulting mixture was stirred at room temperature overnight. The reaction mixture was diluted with ethyl acetate (8 mL), successively washed with water (8 mL), saturated aqueous sodium bicarbonate (2×8 mL) and water (8 mL). The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The crude residue was purified on silica gel using hexanes:ethyl acetate=4:1 to 100% ethyl acetate in a gradient fashion, to isolate the desired product as yellow solid (171.1 mg, 45%). 1H NMR (300 MHz, CDCl3): δ 7.28 (d, 1H), 7.11 (dd, 1H), 6.85 (dd, 1H), 4.11 (br, 2H), 3.74 (t, 2H), 3.72 (br, 1H, OH), 3.36 (t, 2H), 2.92 (t, 4H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935703B2
Source datasetuspto-grants-2011_05
ORD IDord-7b2ec6fd73b649a7b53cde26f00c03aa
Source noteuspto-grants-2011_05