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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885681Generated: November 1, 2026

Sodium Chloride → N-(2,2,6,6-Tetramethyl-4-piperidinyl)acetamide

https://huagongshe.com/reaction/1885681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantAcetic AnhydrideHCID 7918—
Reactant4-Amino-2,2,6,6-tetramethylpiperidineHCID 37524—
SolventTolueneHCID 1140—
ProductN-(2,2,6,6-Tetramethyl-4-piperidinyl)acetamideHCID 100241874.6%

Reaction Steps

A solution of 100.0 grams (64 mmol) of 4-amino-2,2,6,6-tetramethylpiperidine in 150 ml of toluene and a solution of 65.4 grams (64 mmol) of acetic anhydride in 175 ml of toluene are simultaneously added over a 45-minute period to a flask containing 150 ml of toluene. The reaction temperature is maintained at 25°-35° C. by using an ice water bath. The reaction mixture is stirred for 30 minutes after the addition is complete. Solids are separated by filtration, washed with ether and dissolved in 500 ml of water. This aqueous solution is added to a solution of 28 grams of sodium hydroxide in 100 ml of water. A crude solid is isolated by filtration and the filtrate is saturated with solid sodium chloride to precipitate more of the product. The solids are combined, dried and dissolved in warm isopropanol. The alcohol solution is filtered to remove salts, and the filtrate is concentrated to give an oil. The oil is crystallized from heptane to afford 111.0 grams (87% yield) of the title compound as a white solid melting at 100°-102° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05145893
Source datasetuspto-grants-1992_09
ORD IDord-abbf011e00104ac18e61303022b7c0f1
Source noteuspto-grants-1992_09