Brock A. Stenfors, F. Ngassa
Sep 30, 2020
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Journal
European Journal of Chemistry
Abstract
N -Benzyl-4-methylbenzenesulfonamides were prepared via a two-step synthetic process involving the treatment of 4-methylbenzenesulfonyl chloride with a primary amine to give the corresponding 4-methylbenzenesulfonamide. Benzylation of the sulfonamide affords the substituted N -benzyl-4-methylbenzenesulfonamides. The similarities between the two steps of synthesis lend credence to the development of a one-pot synthesis of substituted N -benzyl-4-methylbenzenesulfonamides from 4-methylbenzenesulfonyl chloride. This method was applied to the synthesis of N -allyl- N -benzyl-4-methylbenzenesulfonamide and characterized through spectroscopic and crystallographic means. The crystal structure of N -allyl- N -benzyl-4-methylbenzenesulfonamide was obtained by single-crystal X-ray diffraction. The crystal structure reveals an orthorhombic Pna 2 1 space group with cell parameters a = 18.6919 (18) A, b = 10.5612 (10) A, c = 8.1065 (8) A, V = 1600.3 (3) A 3 and Z = 4, T = 173.15 K, μ(MoKα) = 0.206 mm -1 , Dcalc = 1.251 g/cm 3 , 14455 reflections measured (4.36° ≤ 2Θ ≤ 54.96°), 3619 unique ( R int = 0.0439, R sigma = 0.0429) which were used in all calculations. The final R 1 was 0.0428 (I > 2σ(I)) and wR 2 was 0.1079 (all data). Molecules are linked through C-H···N hydrogen bonds and C-H···π interactions.