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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264133Generated: October 30, 2026

Trimethylamine → HCID 129775352, compound

https://huagongshe.com/reaction/2264133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylamineHCID 1146—
ReactantEpichlorohydrinHCID 7835—
ReactantSodium HydroxideHCID 14798—
ReactantD-GlucosamineHCID 439213—
ProductHCID 129775352HCID 129775352—

Reaction Steps

For the synthesis, pH of the trimethylamine solution was first adjusted to 2.0 to increase the boiling point. Then epoxypropyl chloride at same molar ratio was added dropwise and the pH was maintained at 9 using IM NaOH solution. Glucosamine was then added at same molar ratio and reaction was proceeded by stirring for 24 h. Throughout the reaction pH was maintained at 9.0 product was extracted using ethanol, methanol and tri hydrofluoride and quaternized amino glucosamine was obtained as a dark brown fluffy solid. Structure of newly synthesis was confirmed by elemental analyses and FT-IR. The result of elemental analysis was demonstrated in table 1 and the result of FT-IR was shown in FIG. 1. Bend absorption observed at 1480 cm.sup.-1 in QAGlc by FT-IR, clearly confirmed the quaternization of glucosamine (substitution of N(CH3)3 group).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855188B2
Source datasetuspto-grants-2010_12
ORD IDord-cae812deebfd44039458035069ca4b82
Source noteuspto-grants-2010_12