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1-(4-Hydroxyphenyl)-2-[(4-methylphenyl)sulfonyl]ethanone | 896109-71-0

中文名称
——
中文别名
——
英文名称
1-(4-Hydroxyphenyl)-2-[(4-methylphenyl)sulfonyl]ethanone
英文别名
1-(4-hydroxyphenyl)-2-(4-methylphenyl)sulfonylethanone
1-(4-Hydroxyphenyl)-2-[(4-methylphenyl)sulfonyl]ethanone化学式
CAS
896109-71-0
化学式
C15H14O4S
mdl
——
分子量
290.34
InChiKey
WOZVZBJZOIRWGQ-UHFFFAOYSA-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

计算性质

  • 辛醇/水分配系数(LogP):
    2.6
  • 重原子数:
    20
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    79.8
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    1-(4-Hydroxyphenyl)-2-[(4-methylphenyl)sulfonyl]ethanone 在 ammonium cerium (IV) nitrate 、 氧气 作用下, 以 乙腈 为溶剂, 反应 4.0h, 以90%的产率得到对羟基苯甲酸
    参考文献:
    名称:
    Oxidative cleavage of α-sulfonyl ketones to carboxylic acids with Ce(NH4)2(NO3)6
    摘要:
    Tandem oxidative cleavage of alpha-sulfonyl arylketones 2 with the combination of Ce(NH4)(2)(NO3)(6) and O-2 in MeCN afforded carboxylic acids 3 in moderate to good yields. The plausible reaction mechanism has been discussed. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2014.08.038
  • 作为产物:
    描述:
    2-溴-4'-羟基苯乙酮sodium 4-methylbenzenesulfinate 在 PEG-400 作用下, 反应 0.17h, 以93%的产率得到1-(4-Hydroxyphenyl)-2-[(4-methylphenyl)sulfonyl]ethanone
    参考文献:
    名称:
    Facile polyethylene glycol (PEG-400) promoted synthesis of β-ketosulfones
    摘要:
    An efficient and convenient synthesis of beta-ketosulfones is described. Reaction of an alpha-haloketone with sodium alkyl/aryl sulphinate yields the corresponding beta-ketosulfone promoted by polyethylene glycol (PEG-400) as an efficient reaction medium. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2006.03.181
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文献信息

  • Synthesis of α-iodo β-ketosulfones and α-iodo methylsulfones using iodine monochloride
    作者:N. Suryakiran、T. Srikanth Reddy、V. Suresh、M. Lakshman、Y. Venkateswarlu
    DOI:10.1016/j.tetlet.2006.04.123
    日期:2006.6
    The synthesis of α-iodo β-ketosulfones and α-iodo methylsulfones is described. Reaction of β-ketosulfones with iodine monochloride in acetic acid at room temperature gave the corresponding α-iodo β-ketosulfones, which, on treatment with aqueous alkali, underwent base-induced cleavage to afford α-iodo methylsulfones.
    描述了α-碘β-酮砜和α-碘甲基砜的合成。β-酮砜与一氯化碘在乙酸中于室温下反应,得到相应的α-碘β-酮砜,将其用碱水溶液处理,进行碱诱导的裂解,得到α-碘甲基甲砜。
  • Oxidative cleavage of α-sulfonyl ketones to carboxylic acids with Ce(NH4)2(NO3)6
    作者:Meng-Yang Chang、Chung-Yu Tsai
    DOI:10.1016/j.tetlet.2014.08.038
    日期:2014.10
    Tandem oxidative cleavage of alpha-sulfonyl arylketones 2 with the combination of Ce(NH4)(2)(NO3)(6) and O-2 in MeCN afforded carboxylic acids 3 in moderate to good yields. The plausible reaction mechanism has been discussed. (C) 2014 Elsevier Ltd. All rights reserved.
  • Facile polyethylene glycol (PEG-400) promoted synthesis of β-ketosulfones
    作者:N. Suryakiran、T. Srikanth Reddy、K. Ashalatha、M. Lakshman、Y. Venkateswarlu
    DOI:10.1016/j.tetlet.2006.03.181
    日期:2006.6
    An efficient and convenient synthesis of beta-ketosulfones is described. Reaction of an alpha-haloketone with sodium alkyl/aryl sulphinate yields the corresponding beta-ketosulfone promoted by polyethylene glycol (PEG-400) as an efficient reaction medium. (c) 2006 Elsevier Ltd. All rights reserved.
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