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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888701Generated: October 30, 2026

Hydrochloric Acid → HCID 15428431, compound

https://huagongshe.com/reaction/888701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant7-(3-Carboxy-1-oxopropyl)-γ-oxo-9H-fluorene-2-butanoic acidHCID 58776022—
SolventWaterHCID 962—
SolventDiethylene GlycolHCID 8117—
ProductHCID 15428431HCID 15428431—

Reaction Conditions

Temperature110 °C

Reaction Steps

In an argon-purged flask 2,7-di(3-carboxy-propionyl)fluorene (12.8 g, 0.035 mol) was suspended in diethylene glycol (150 mL). The flask was placed in a room temperature oil bath then NaOH (14 g, 0.35 mol) and an 80% solution of hydrazine hydrate (13.1 mL, 0.21 mol) were added successively. The reaction mixture was slowly heated to 110° C. and refluxed for approximately two hours. The reaction temperature was raised to 200° C. with removal of water during the heating process. After three hours at 200° C. reaction temperature the reaction was cooled to approximately 60° C. The reaction mixture was carefully poured into water (500 mL) and the mixture was acidified to pH 2 with concentrated HCl. The product was filtered and washed with water. The product was dissolved in warm NaOH solution (0.5M) and precipitated by acidification to pH 2 with HCl. The product was filtered and washed with water (Yield 10.9 g, 92%). 1H-NMR (d6-DMSO): δ (ppm) 12.0 (s, 2H, COOH); 7.8 (m, 2H, Ar); 7.4 (s, 2H, Ar); 7.2 (m, 2H, Ar); 3.9 (s, 2H, CH2); 2.7 (t, 4H, CH2); 2.3 (t, 4H, CH2); 1.8 (m, 4H, CH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08252275B2
Source datasetuspto-grants-2012_08
ORD IDord-13128445456042d7a49241307e09823b
Source noteuspto-grants-2012_08