NMR data for compound 34. N-(pyridin-2-yl)benzamide
DOI: 10.14469/hpc/14743 Metadata
Created: 2024-11-02 07:04
Last modified: 2025-02-08 14:22
License: Creative Commons: Public Domain Dedication 1.0
Funding: (none given)
Description
Synthesised according to the general procedure, reaction for 44 hours. Purified by flash column chromatography (EtOAc in hexanes, 10% à 70%). Yield = 402 mg crystalline white solid, 40%. Analytical data is in accordance with literature reports.20 1H NMR (700 MHz, CDCl3) δ (ppm) = 8.91 (s, 1H), 8.40 (dt, J = 8.4 Hz, 1 Hz, 1H), 8.20 (dd, J = 5 Hz, 1 Hz), 1 H), 7.91-7.93 (m, 2H), 7.75 (ddd, J = 8.4, 7.4, 1.9 Hz, 1H), 7.56 (tt, J = 7.4, 1.2 Hz, 1H), 7.48 (t, 7.8 Hz, 2H), 7.04 (ddd, J = 7.3, 4.9, 1 Hz, 1H). 13C NMR (176 MHz, CDCl3) δ (ppm) = δ 166.1, 151.8, 147.9, 138.7, 134.5, 132.4, 128.9, 127.5, 120.0, 114.5. HRMS [C12H10N¬O2+H]+: Calculated = 199.0866, found 199.0865 Melting point: 78 – 82 °C
Member of collection / collaboration
DOI | Description |
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10.14469/hpc/14635 | Borate-Catalysed Direct Amidation Reactions of Coordinating Substrates. NMR data |
Members
DOI | Description |
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10.14469/hpc/14811 | NMR data for compound 34. N-(pyridin-2-yl)benzamide 1H |
10.14469/hpc/14812 | NMR data for compound 34. N-(pyridin-2-yl)benzamide 13C. |
Subject Keywords
Keyword | Value |
---|---|
inchi | InChI=1S/C12H10N2O/c15-12(10-6-2-1-3-7-10)14-11-8-4-5-9-13-11/h1-9H,(H,13,14,15) |
Inchikey | LZIJKEIPCFEOLH-UHFFFAOYSA-N |