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15871-63-3

ETHANONE,1-[4-(2-HYDROXYETHYL)-1-PIPERIDINYL]- synthesis

3synthesis methods
-

Yield:15871-63-3 86%

Reaction Conditions:

in dichloromethane; for 2 h;Cooling with ice;

Steps:

3 In the synthetic route, the specific process of intermediate (9) (hereinafter referred to as compound 9) is:

Under an ice bath, compound 5 (abbreviation of (5) in the synthetic route) (2.00g, 15.5mmol) was dissolved in DC M solution (8mL), and acetic anhydride (1.10g, 17.0mmol) was slowly dropped into it, Stir under ice bath for 2 hours. After the reaction was completed, the reaction solution was washed with saturated sodium chloride (8 mL), dried over anhydrous sodium sulfate and concentrated to obtain compound 9 (colorless oily liquid, 2.28 g, 86%).

References:

CN113264937,2021,A Location in patent:Paragraph 0077-0079; 0083-0085