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Molbank
Volume 2021
Issue 2
10.3390/M1198
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Short Note

N-[(1R)-1-(4-Chlorophenyl)ethyl]-Cyanamide

by
Rebeca González-Fernández
,
Pascale Crochet
and
Victorio Cadierno
*
Departamento de Química Orgánica e Inorgánica, Facultad de Química, Universidad de Oviedo, Julián Clavería 8, E-33006 Oviedo, Spain
*
Author to whom correspondence should be addressed.
Molbank 2021, 2021(2), M1198; https://doi.org/10.3390/M1198
Submission received: 17 March 2021 / Revised: 24 March 2021 / Accepted: 25 March 2021 / Published: 26 March 2021
(This article belongs to the Section Organic Synthesis and Biosynthesis)
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Abstract

The title compound was synthesized by electrophilic cyanation of commercially available (R)-4-chloro-α-methylbenzylamine with cyanogen bromide in diethyl ether, and isolated as a yellow oil in 84% yield. It was characterized by 1H and 13C{1H] NMR, IR, HRMS, and specific rotation measurements.
Keywords: cyanamides; electrophilic cyanation; cyanogen bromide; amines; chiral molecules cyanamides; electrophilic cyanation; cyanogen bromide; amines; chiral molecules

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MDPI and ACS Style

González-Fernández, R.; Crochet, P.; Cadierno, V. N-[(1R)-1-(4-Chlorophenyl)ethyl]-Cyanamide. Molbank 2021, 2021, M1198. https://doi.org/10.3390/M1198

AMA Style

González-Fernández R, Crochet P, Cadierno V. N-[(1R)-1-(4-Chlorophenyl)ethyl]-Cyanamide. Molbank. 2021; 2021(2):M1198. https://doi.org/10.3390/M1198

Chicago/Turabian Style

González-Fernández, Rebeca, Pascale Crochet, and Victorio Cadierno. 2021. "N-[(1R)-1-(4-Chlorophenyl)ethyl]-Cyanamide" Molbank 2021, no. 2: M1198. https://doi.org/10.3390/M1198

APA Style

González-Fernández, R., Crochet, P., & Cadierno, V. (2021). N-[(1R)-1-(4-Chlorophenyl)ethyl]-Cyanamide. Molbank, 2021(2), M1198. https://doi.org/10.3390/M1198

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