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ChemicalBook CAS DataBase List Lidocaine hydrochloride

Lidocaine hydrochloride synthesis

4synthesis methods
-

Yield:73-78-9 100%

Reaction Conditions:

with hydrogenchloride in diethyl ether;

Steps:

Preparationof Lidocaine hydrochloride monohydrate:

Dry HCl was bubbled through a solution of lidocaine (3 g) in anhydrous ether (75 cm3). The salt precipitated immediately; passage of HCl continued until no further precipitate was formed.The salt was filtered and washed with liberal excess of ether to obtain it in almost quantitative yield. A portion of the salt was kept in the open atmosphere (72 h, next to a beaker containingwater as source of moisture) to obtain Lidocaine.HCl.H2O (mp is 73-74 °C in excellent agreement with literature reported mp of 73-74°C [1]). Another portion was dried under vacuum at 50°C until the mp of the salt reaches aconstant value indicating the formation of the anhydrous salt Lidocaine.HCl (closed capillary mp is 131-133°C, as compared to Lit. [2] mp of 127-132°C) for NMR spectral comparison.

References:

Badawi, Hassan M.;F?rner, Wolfgang;Ali, Shaikh A. [Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy,2016,vol. 152,p. 92 - 100] Location in patent:supporting information

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