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3-硝基-2-丁醇 | 6270-16-2

中文名称
3-硝基-2-丁醇
中文别名
3-硝基-丁醇
英文名称
3-nitrobutan-2-ol
英文别名
(2RS,3RS)-3-nitro-butan-2-ol;threo-dl-3-Nitro-butan-2-ol;2-Butanol, 3-nitro-, (R*,R*)-;(2R,3R)-3-nitrobutan-2-ol
3-硝基-2-丁醇化学式
CAS
6270-16-2;82978-01-6;82978-02-7
化学式
C4H9NO3
mdl
——
分子量
119.12
InChiKey
OJVOGABFNZDOOZ-QWWZWVQMSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 熔点:
    21.25°C (estimate)
  • 沸点:
    55 °C0.5 mm Hg(lit.)
  • 密度:
    1.1 g/mL at 25 °C(lit.)
  • 闪点:
    196 °F

计算性质

  • 辛醇/水分配系数(LogP):
    0.2
  • 重原子数:
    8
  • 可旋转键数:
    1
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    66
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 危险品标志:
    Xi
  • 安全说明:
    S24/25,S26,S36/37/39
  • 危险类别码:
    R36/37/38
  • WGK Germany:
    3

SDS

SDS:f939d70d904efdc9c7c2e172d53d63af
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反应信息

  • 作为反应物:
    描述:
    3-硝基-2-丁醇1-Alapha-萘异氰酸酯 生成 threo-dl-3-Nitro-2-<α-naphthylcarbamoyloxy>-butan
    参考文献:
    名称:
    Nitrations with Acetyl Nitrate. I. The Nature of the Nitrating Agent and the Mechanism of Reaction with Simple Alkenes
    摘要:
    DOI:
    10.1021/ja01499a029
  • 作为产物:
    描述:
    (2RS,3RS)-2-acetoxy-3-nitro-butane 生成 3-硝基-2-丁醇
    参考文献:
    名称:
    Nitrations with Acetyl Nitrate. I. The Nature of the Nitrating Agent and the Mechanism of Reaction with Simple Alkenes
    摘要:
    DOI:
    10.1021/ja01499a029
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文献信息

  • Zinc metal–organic frameworks: efficient catalysts for the diastereoselective Henry reaction and transesterification
    作者:Anirban Karmakar、M. Fátima C. Guedes da Silva、Armando J. L. Pombeiro
    DOI:10.1039/c4dt00219a
    日期:——

    Three new amidoterephthalate ligands are utilized to synthesize three new zinc(ii) metal–organic frameworks which act as heterogeneous catalysts for the diastereoselective nitroaldol (Henry) and transesterification reactions.

    三种新的酰胺基对苯二甲酸配体被用于合成三种新的(II)属-有机框架,这些框架作为非均相催化剂用于选择性立体异构的硝基醛(Henry)和酯交换反应。
  • Synthesis of Metallomacrocycle and Coordination Polymers with Pyridine-Based Amidocarboxylate Ligands and Their Catalytic Activities towards the Henry and Knoevenagel Reactions
    作者:Anirban Karmakar、Guilherme M. D. M. Rúbio、M. Fátima C. Guedes da Silva、Armando J. L. Pombeiro
    DOI:10.1002/open.201800170
    日期:2018.11
    (H2L) with zinc(II), cadmium(II), and samarium(III) nitrates were studied, and the obtained compounds, [Zn(1κO:2κO′‐L)(H2O)2]n (1), [Cd(1κO2:2κO2‐L)(H2O)2]2⋅6n H2O⋅ n C4H8O2⋅1.5n DMF (2), and [Sm(1κO:2κO′O′′:3κO′′′‐L)(NO3)(H2O)(dmf)]nn DMF (3), were characterized by elemental analysis, FTIR spectroscopy, thermogravimetric analysis, and X‐ray single‐crystal diffraction. Compounds 1 and 3 have 1D zigzag‐
    研究了3,3'-(吡啶-2,6-二羰基)双(氮杂二基)}二苯甲酸 (H 2 L) 与硝酸 (II)、硝酸镉 (II) 和硝酸钐 (III) 的反应,以及所得化合物[Zn(1κ O :2κ O′ ‐L)(H 2 O) 2 ] n ( 1 ), [Cd(1κ O 2 :2κ O 2 ‐L)(H 2 O) 2 ] 2 ⋅ 6 n  H 2 O ⋅ n  C 4 H 8 O 2 ⋅ 1.5 n  DMF ( 2 ), 和 [Sm(1κ O :2κO ′ O ′′ :3κ O′′′ ‐L)(NO 3 )(H 2 O)(DMF)] n ⋅ n  DMF ( 3 ),通过元素分析、FTIR 光谱、热重分析和 X 射线单晶衍射进行表征。化合物1和3分别具有一维锯齿形和双链型结构,而2则具有双核属大环配合物。配体(L 2− )以不同的构象取向,即1为syn-syn,2和3为anti-anti。化合物1
  • Amide functionalized metal–organic frameworks for diastereoselective nitroaldol (Henry) reaction in aqueous medium
    作者:Anup Paul、Anirban Karmakar、M. Fátima C. Guedes da Silva、Armando J. L. Pombeiro
    DOI:10.1039/c5ra14637b
    日期:——

    The metal–organic frameworks [Zn2(L)2(1,4-BDC)]n·2n(DMF) (L = 4-(pyridin-4-ylcarbamoyl)benzoate; BDC = benzenedicarboxylate) and [Cu(L)2]n·4n(DMF)·n(H2O) work as catalysts for the diastereoselective nitroaldol reaction in aqueous medium.

    属有机框架[Zn2(L)2(1,4-BDC)]n·2n(DMF)(其中L = 4-(吡啶-4-基甲酰)苯甲酸根;BDC = 苯二甲酸根)和[Cu(L)2]n·4n(DMFn(H2O)可作为介质中对映选择性硝基醛醇反应的催化剂。
  • Zinc amidoisophthalate complexes and their catalytic application in the diastereoselective Henry reaction
    作者:Anirban Karmakar、M. Fátima C. Guedes da Silva、Susanta Hazra、Armando J. L. Pombeiro
    DOI:10.1039/c4nj02371d
    日期:——

    5-Propionamidoisophthalic acid and 5-benzamidoisophthalic acid are used to synthesize new zinc(ii) complexes which act as heterogeneous catalysts for the diastereoselective nitroaldol (Henry) reaction.

    5-丙酰胺基异苯二甲酸和5-苯甲酰胺基异苯二甲酸被用于合成新的(II)配合物,这些配合物作为非均相催化剂用于立体选择性的硝基醇(Henry)反应。
  • Metal–Organic Frameworks with Pyridyl-Based Isophthalic Acid and Their Catalytic Applications in Microwave Assisted Peroxidative Oxidation of Alcohols and Henry Reaction
    作者:Anirban Karmakar、Luísa M. D. R. S. Martins、Susanta Hazra、M. Fátima C. Guedes da Silva、Armando J. L. Pombeiro
    DOI:10.1021/acs.cgd.5b01178
    日期:2016.4.6
    building unit. These frameworks act as heterogeneous polymeric solid catalysts (the most effective one being the copper MOF 1) for solvent-free microwave assisted peroxidative oxidation of primary and secondary alcohols. They also effectively catalyze the nitroaldol (Henry) reaction of different aldehydes with nitroalkanes in water. These MOF-based heterogeneous catalysts can be easily recovered and reused
    研究了5-(吡啶-4-基甲基)基}间苯二甲酸(H 2 L1)与(II),(II)和(II)的反应,并获得了属有机骨架(MOF) [Cu(L1)(DMF)}·DMF·H 2 O] n(1),[Zn(L1)(H 2 O)] n(2)和[Cd(L1)] n(3)分别是通过元素分析,傅立叶变换红外光谱和X射线单晶衍射进行表征。如X射线晶体学所示,获得了新颖的有机-无机配位混合驱动组装体,这些组装体表现出不同的二维和三维(2D和3D)聚合物结构。化合物1和2具有2D结构,而化合物3具有3D网络型聚合物,该聚合物具有双属核,可作为辅助构建单元。这些骨架充当多相聚合物固体催化剂(最有效的一种是MOF 1),用于无溶剂微波辅助伯醇和仲醇的过氧化氧化。它们还可以有效催化中的不同醛与硝基烷的硝基醛(亨利)反应。这些基于MOF的非均相催化剂可以轻松回收和再利用,至少连续几个循环,而不会损失活性。
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