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ChemicalBook CAS DataBase List (9H-fluoren-9-yl)methyl piperidine-1-carboxylate
207558-19-8

(9H-fluoren-9-yl)methyl piperidine-1-carboxylate synthesis

7synthesis methods
-

Yield:207558-19-8 77%

Reaction Conditions:

in neat (no solvent) at 20; for 0.0833333 h;Sonication;Irradiation;Green chemistry;

Steps:

General procedure of N-Fmoc protection on amines derivatives promoted by ultrasound irradiations

General procedure: Amine (1 mmol) and Fmoc-Cl (1.1 mmol) were placed in a glass tube under neat conditions and were sonicated for a suitable time (as indicated in Tables 1, 2 and 3). All reactions were performed in a water bath at room temperature. After completion of the reaction (as indicated by TLC), 5 cm3 of diethyl ether was added to the mixture. The N-Fmoc derivatives were crystallized and were obtained in good to excellent yields. Purification of the product was accomplished by recrystallization from diethyl ether.

References:

Mansouri, Rachida;Aouf, Zineb;Lakrout, Salah;Berredjem, Malika;Aouf, Nour-Eddine [Journal of the Brazilian Chemical Society,2016,vol. 27,# 3,p. 546 - 550]