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4-acetyloxy-2-aminobenzenesulfonic acid | 1245708-00-2

中文名称
——
中文别名
——
英文名称
4-acetyloxy-2-aminobenzenesulfonic acid
英文别名
——
4-acetyloxy-2-aminobenzenesulfonic acid化学式
CAS
1245708-00-2
化学式
C8H9NO5S
mdl
——
分子量
231.229
InChiKey
RVUUXCBCURTLHL-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):
    0.44
  • 重原子数:
    15.0
  • 可旋转键数:
    2.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    106.69
  • 氢给体数:
    2.0
  • 氢受体数:
    5.0

反应信息

  • 作为产物:
    描述:
    1,3-苯并噻唑-5-基乙酸酯 在 [RuCl(P(C6H5)3)2(O(C6H4)NCH(C4H3N))] 、 bromamine B 、 sodium hydroxide 作用下, 以 乙腈 为溶剂, 反应 4.67h, 以95%的产率得到4-acetyloxy-2-aminobenzenesulfonic acid
    参考文献:
    名称:
    Development of an efficient ruthenium catalyzed synthetic process and mechanism for the facile conversion of benzothiazoles to orthanilic acids
    摘要:
    Ruthenium-Schiff base complex catalyzed efficient protocol has been developed for the synthesis of orthanilic acids from benzothiazoles in good to excellent yields using N-haloamines. Hexa-coordinated ruthenium complex with Schiff base and triphenylphosphine ligands has been prepared and its catalytic function was invented for the synthesis of orthanilic acids. The synthetic process utilizes our efficient method for the selective and preferential oxidation of thiazole ring of benzothiazoles using N-haloamines without effecting phenyl ring. The detailed catalytic, mechanistic and kinetic investigations have been made for the synthetic reactions. Solvent isotope studies have been made in H2O-D2O and the reactions were carried out at different temperatures. Under the identical set of conditions, the kinetics of catalyzed reactions has been compared with uncatalyzed reactions and found that the catalyzed reactions are 9-11 folds faster. The catalytic constants (K-c) have been calculated for each N-haloamine at different temperatures and the values of activation parameters with respect to the catalyst have been evaluated. Spectroscopic evidence for the formation of 1:1 complex between N-haloamine and ruthenium has been obtained. The observed results have been explained by a plausible mechanism and the related rate law has been deduced. (C) 2010 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.molcata.2010.06.006
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文献信息

  • The Efficient Palladium-Catalyzed Selective t Synthesis of Benzenesulfonic Acids
    作者:Rajenahally V. Jagadeesh、Y. Sree Sandhya、P. Karthikeyan、S. Sudhakar Reddy、P. Pradeep Kumar Reddy、M. Viniod Kumar、K. T. Prabhu Charan、R. Narender、P. R. Bhagat
    DOI:10.1080/00397911.2010.502991
    日期:2011.8.15
    [image omitted] Palladium-catalyzed synthetic methodology has been developed for the synthesis of 2-aminobenzenesulfonic acids from benzothiazoles in good to excellent yields using chloramine-B in alkaline (pH 12) acetonitrile/water (1:1) at 80 degrees C.
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同类化合物

马来酰亚胺四聚乙二醇CH2CH2COOPFPESTER 马来酰亚胺六聚乙二醇CH2CH2COOPFPESTER 马来酰亚胺-酰胺-PEG8-四氟苯酚酯 马来酰亚胺-四聚乙二醇-五氟苯酯 马来酰亚胺-三聚乙二醇-五氟苯酚酯 靛酚乙酸酯 阿立哌唑标准品002 间硝基苯基戊酸酯 间氯苯乙酸乙酯 间乙酰苯甲酸 钾4-乙酰氧基苯磺酸酯 酚醛乙酸酯 邻苯二酚二乙酸酯 邻甲苯基环己甲酸酯 邻甲氧基苯乙酸酯 辛酸苯酯 辛酸对甲苯酚酯 辛酸五氯苯基酯 辛酸-(3-氯-苯基酯) 辛酰溴苯腈 苯酰胺,3,4-二(乙酰氧基)-N-[6-氨基-1,2,3,4-四氢-1-(4-甲氧苯基)-3-甲基-2,4-二羰基-5-嘧啶基]- 苯酚-乳酸 苯酚,4-异氰基-,乙酸酯(ester) 苯酚,4-[(四氢-2H-吡喃-2-基)氧代]-,乙酸酯 苯酚,3-(1,1-二甲基乙基)-,乙酸酯 苯酚,2-溴-3-(二溴甲基)-5-甲氧基-,乙酸酯 苯甲醇,4-(乙酰氧基)-3,5-二甲氧基- 苯甲酸,4-(乙酰氧基)-2-氟- 苯氧基氯乙酸苯酯 苯基金刚烷-1-羧酸酯 苯基氰基甲酸酯 苯基庚酸酯 苯基庚-6-炔酸酯 苯基己酸酯 苯基呋喃-2-羧酸酯 苯基吡啶-2-羧酸酯 苯基十一碳-10-烯酸酯 苯基乙醛酸酯 苯基乙酸酯-d5 苯基丙二酸单苯酯 苯基丙-2-炔酸酯 苯基丁-2,3-二烯酸酯 苯基4-乙基环己烷羧酸 苯基3-乙氧基-3-亚氨基丙酸盐 苯基2-(苯磺酰基)乙酸酯 苯基2-(4-甲氧基苯基)乙酸酯 苯基2-(2-甲氧基苯基)乙酸酯 苯基2-(2-甲基苯基)乙酸酯 苯基-乙酸-(2-甲酰基-苯基酯) 苯基-乙酸-(2-环己基-苯基酯)