3-硝基二苯甲烷

3-硝基二苯甲烷
識別
CAS號	5840-41-5
性質
化學式	C13H11NO2
摩爾質量	213.23 g·mol−1
沸點	164—166 °C（437—439 K）（3 torr）
	若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。

3-硝基二苯甲烷是一種有機化合物，化學式為C₁₃H₁₁NO₂。它可由3-硝基苄溴和苯硼酸在碳酸鈉和鈀催化劑的存在下反應得到，^[2]該偶聯反應也可使用氯化苄和3-硝基苯硼酸為原料進行反應。^[3]它可以被氯化亞錫還原為3-氨基二苯甲烷。^[4]Ag/C奈米顆粒可以催化它和氧氣的反應，產物為3-硝基二苯甲酮。^[5]

參考文獻[編輯]

^ Kim Huard, Hélène Lebel. N ‐Tosyloxycarbamates as Reagents in Rhodium‐Catalyzed CH Amination Reactions. Chemistry - A European Journal. 2008-07-07, 14 (20): 6222–6230 [2021-12-24]. doi:10.1002/chem.200702027 （英語）.
^ Michael J. Burns, Ian J. S. Fairlamb, Anant R. Kapdi, Petr Sehnal, Richard J. K. Taylor. Simple Palladium(II) Precatalyst for Suzuki−Miyaura Couplings: Efficient Reactions of Benzylic, Aryl, Heteroaryl, and Vinyl Coupling Partners. Organic Letters. 2007-12-01, 9 (26): 5397–5400 [2021-12-24]. ISSN 1523-7060. doi:10.1021/ol702291r. （原始內容存檔於2021-12-24）（英語）.
^ Nicolas Henry, Cécile Enguehard-Gueiffier, Isabelle Thery, Alain Gueiffier. One-Pot Dual Substitutions of Bromobenzyl Chloride, 2-Chloromethyl-6-halogenoimidazo[1,2- a ]pyridine and -[1,2- b ]pyridazine by Suzuki-Miyaura Cross-Coupling Reactions. European Journal of Organic Chemistry. 2008-10, 2008 (28): 4824–4827 [2021-12-24]. doi:10.1002/ejoc.200800544 （英語）.
^ Mark A. Dekeyser, David M. Borth, Richard C. Moore, Anupama Mishra. Quantitative structure-activity relationships in acaricidal 4H-1,3,4-oxadiazin-5(6H)-ones. Journal of Agricultural and Food Chemistry. 1991-02, 39 (2): 374–379 [2021-12-24]. ISSN 0021-8561. doi:10.1021/jf00002a030 （英語）.
^ Shuangxi Guo, Qi Zhang, Hongbo Li, Huifang Guo, Wei He. Ag/C nanoparticles catalysed aerobic oxidation of diaryl and aryl(hetero) methylenes into ketones. Nano Research. 2017-09, 10 (9): 3261–3267 [2021-12-24]. ISSN 1998-0124. doi:10.1007/s12274-017-1676-2 （英語）.

[1] Kim Huard, Hélène Lebel. N ‐Tosyloxycarbamates as Reagents in Rhodium‐Catalyzed CH Amination Reactions. Chemistry - A European Journal. 2008-07-07, 14 (20): 6222–6230 [2021-12-24]. doi:10.1002/chem.200702027 （英語）.

[2] Michael J. Burns, Ian J. S. Fairlamb, Anant R. Kapdi, Petr Sehnal, Richard J. K. Taylor. Simple Palladium(II) Precatalyst for Suzuki−Miyaura Couplings: Efficient Reactions of Benzylic, Aryl, Heteroaryl, and Vinyl Coupling Partners. Organic Letters. 2007-12-01, 9 (26): 5397–5400 [2021-12-24]. ISSN 1523-7060. doi:10.1021/ol702291r. （原始內容存檔於2021-12-24）（英語）.

[3] Nicolas Henry, Cécile Enguehard-Gueiffier, Isabelle Thery, Alain Gueiffier. One-Pot Dual Substitutions of Bromobenzyl Chloride, 2-Chloromethyl-6-halogenoimidazo[1,2- a ]pyridine and -[1,2- b ]pyridazine by Suzuki-Miyaura Cross-Coupling Reactions. European Journal of Organic Chemistry. 2008-10, 2008 (28): 4824–4827 [2021-12-24]. doi:10.1002/ejoc.200800544 （英語）.

[4] Mark A. Dekeyser, David M. Borth, Richard C. Moore, Anupama Mishra. Quantitative structure-activity relationships in acaricidal 4H-1,3,4-oxadiazin-5(6H)-ones. Journal of Agricultural and Food Chemistry. 1991-02, 39 (2): 374–379 [2021-12-24]. ISSN 0021-8561. doi:10.1021/jf00002a030 （英語）.

[5] Shuangxi Guo, Qi Zhang, Hongbo Li, Huifang Guo, Wei He. Ag/C nanoparticles catalysed aerobic oxidation of diaryl and aryl(hetero) methylenes into ketones. Nano Research. 2017-09, 10 (9): 3261–3267 [2021-12-24]. ISSN 1998-0124. doi:10.1007/s12274-017-1676-2 （英語）.

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