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S-(6-acetamido-2-naphthyl) N,N-dimethylthiocarbamate | 114646-81-0

中文名称
——
中文别名
——
英文名称
S-(6-acetamido-2-naphthyl) N,N-dimethylthiocarbamate
英文别名
S-(N-acetyl-6-amino-2-naphthyl)-N,N-dimethylthiocarbamate;S-(6-acetamidonaphthalen-2-yl) N,N-dimethylcarbamothioate
S-(6-acetamido-2-naphthyl) N,N-dimethylthiocarbamate化学式
CAS
114646-81-0
化学式
C15H16N2O2S
mdl
——
分子量
288.37
InChiKey
UROZXNZBAOFAIA-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):
    2.7
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    74.7
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Thiocarbamates and their derivatives
    申请人:Hoechst Celanese Corporation
    公开号:US05157142A1
    公开(公告)日:1992-10-20
    A process is provided for preparing N-acyl-aminothiophenols, e.g., N-acetyl-para-aminothiophenol, or aminothiophenols, e.g., para-aminothiophenol, by reacting a hydroxy aromatic ketone, e.g., 4-hydroxyacetophenone (4-HAP), with hydroxylamine or a hydroxylamine salt, to form the oxime of the ketone, subjecting the oxime to a Beckmann rearrangement in the presence of a catalyst to form the N-acyl-hydroxy aromatic amine, e.g., N-acetyl-para-aminophenol (APAP), reacting the N-acyl-hydroxy aromatic amine with an N,N-di (organo) thiocarbamoyl halide, e.g., N,N-dimethylthiocarbamoyl chloride, to form an O-(N-acyl-aminoaryl)-N,N-di (organo) thiocarbamate, e.g., O-(N-acetyl-para-aminophenyl)-N,N-dimethylthiocarbamate, pyrolytically rearranging the O-(N-acyl-aminoaryl)-N,N-di (organo) thiocarbamate to form an S-(N-acyl-aminoaryl)-N,N-di (organo) thiocarbamate, e.g., S-(N-acetyl-para-aminophenyl)-N,N-dimethylthiocarbamate, and hydrolyzing the latter compound to obtain the N-acyl aminothiophenol or aminothiophenol. The N-acyl aminothiophenol may be reacted with an acylating agent to form the N,S-diacyl-aminothiophenol, e.g., N,S-diacetyl-p-aminothiophenol, or may be further hydrolyzed to the aminothiophenol, e.g., p-aminothiophenol.
    提供了一种制备N-酰基氨基硫酚,例如N-乙酰基对氨基硫酚,或氨基硫酚,例如对氨基硫酚的方法,通过将羟基芳香酮,例如4-羟基乙酰苯酮(4-HAP),与羟胺或羟胺盐反应,形成酮的肟,将肟在催化剂存在下进行贝克曼重排反应,形成N-酰基-羟基芳香胺,例如N-乙酰基对-氨基苯酚(APAP),将N-酰基-羟基芳香胺与N,N-二(有机)硫代氨基卤化物,例如N,N-二甲基硫代氨基氯化物,反应形成O-(N-酰基氨基芳基)-N,N-二(有机)硫代氨酸酯,例如O-(N-乙酰基对-氨基苯基)-N,N-二甲基硫代氨酸酯,通过热解重排O-(N-酰基氨基芳基)-N,N-二(有机)硫代氨酸酯形成S-(N-酰基氨基芳基)-N,N-二(有机)硫代氨酸酯,例如S-(N-乙酰基对-氨基苯基)-N,N-二甲基硫代氨酸酯,将后一化合物水解得到N-酰基氨基硫酚或氨基硫酚。N-酰基氨基硫酚可以与酰化剂反应形成N,S-二酰基氨基硫酚,例如N,S-二乙酰-p-氨基硫酚,或进一步水解为氨基硫酚,例如p-氨基硫酚。
  • Process for producing aminothiophenols and their derivatives
    申请人:CELANESE CORPORATION
    公开号:EP0251552A2
    公开(公告)日:1988-01-07
    A process is provided for preparing N-acyl-aminothiophenols, e.g., N-acetyl-para-aminothiophenol, or aminothiophenols, e.g., para-aminothiophenol, by reacting a hydroxy aromatic ketone, e.g., 4-hydroxyacetophenone (4-HAP), with hydroxylamine or a hydroxylamine salt, to form the oxime of the ketone, subjecting the oxime to a Beckmann rearrangement in the presence of a catalyst to form the N-acyl-hydroxy aromatic amine, e.g., N-acetyl-para-aminophenol (APAP), reacting the N-acyl-hydroxyaromatic amine with an N,N-di-(organo) thiocarbamoyl halide, e.g., N,N-dimethylthiocarbamoyl chloride, to form an O-(N-acyl-aminoaryl)-N,N-di-(organo) thiocarbamate, e.g., 0-(N-acetyl-para-aminophenyl)-N,N-dimethylthiocarbamate, pyrolytically rearranging the 0-(N-acyl-aminoaryl)-N,N-di(organo)thiocarbamate to form an S-(N-acyl-aminoaryl)-N,N-di(organo)-thiocarbamate, e.g., S-(N-acetyl-para-aminophenyl)-N,N-dimethylthiocarbamate, and hydrolyzing the latter compound to obtain the N-acyl aminothiophenol or aminothiophenol. The N-acyl aminothiophenol may be reacted with an acylating agent to form the N,S-diacyl-aminothiophenol, e.g., N,S-diacetyl-p-aminothiophenol, or may be further hydrolyzed to the aminothiophenol, e.g., p-aminothiophenol.
    本发明提供了一种制备 N-酰基氨基苯硫酚(如 N-乙酰基对氨基苯硫酚)或氨基苯硫酚(如对氨基苯硫酚)的工艺,该工艺通过使羟基芳香族酮(如 4-羟基苯乙酮(4-HAP))与羟胺或羟胺盐反应形成酮的肟,使肟进行贝克曼重排、4-羟基苯乙酮(4-HAP)与羟胺或羟胺盐反应生成酮的肟,在催化剂存在下使肟发生贝克曼重排反应生成 N-酰基-羟基芳香胺,如对位氨基苯硫酚、N-acetyl-para-aminophenol (APAP),使 N-酰羟基芳胺与 N,N-二(有机)硫代氨基甲酰卤反应,例如N,N-二甲基硫代氨基甲酰氯反应,生成 O-(N-酰基-氨基芳基)-N,N-二(有机)硫代氨基甲酸酯,例如0-(N-乙酰基-对氨基苯基)-N,N-二甲基硫代氨基甲酸酯,热解重新排列 0-(N-酰基-氨基芳基)-N,N-二(有机)硫代氨基甲酸酯,形成 S-(N-酰基-氨基芳基)-N,N-二(有机)硫代氨基甲酸酯,例如S-(N-乙酰基-对氨基苯基)-N,N-二甲基硫代氨基甲酸酯,水解后的化合物得到 N-酰基氨基苯硫酚或氨基苯硫酚。N-acyl 氨基苯硫酚可与酰化剂反应生成 N,S-二乙酰基-氨基苯硫酚,如 N,S-二乙酰基-对氨基苯硫酚,或进一步水解生成氨基苯硫酚,如对氨基苯硫酚。
  • Method for producing aminothiophenols and their derivatives
    申请人:HOECHST CELANESE CORPORATION
    公开号:EP0269434A1
    公开(公告)日:1988-06-01
    A method is provided for preparing N-acyl-aminothiophenols, e.g., N-acetyl-para-aminothiophenol, or aminothiophenols, e.g., para-aminothiophenol, by reacting any of certain sulfur-containing ketones, viz., an S-(acylaryl) N,N-di(organo)thiocarbamate, e.g., S-(4'-acetophenyl)-N,N-dimethylthiocarbamate, an acylthiophenol acylate ester, e.g., 4-acetothiophenol acetate, or a free acylthiophenol, e.g., 4-acetothiophenol with hydroxylamine or a hydroxylamine salt, to form the oxime of the ketone, subjecting the oxime to a Beckmann rearrangement in the presence of a catalyst to form an S-(N-acyl-aminoaryl) N,N-di(organo)thiocarbamate, e.g., S-(N-acetyl-para-aminophenyl) N,N-dimethylthiocarbamate, an N,S-diacylaminothiophenol, e.g., N,S-diacetyl-para-aminothiophenol, or an N-acyl aminothiophenol, e.g., N-acetyl-para-amino- thiophenol, respectively. The S-(N-acyl-aminoaryl) N,N-di(organo)thiocarbamate may be hydrolyzed to the N-acyl amino- thiophenol or aminothiophenol. The S-(acylaryl) N,N-di(organo)thiocarbamate may be produced by reacting a hydroxy aromatic ketone, e.g., 4-hydroxyacetophenone (4-HAP) with an N,N-di(organo)thiocarbamoyl halide, e.g., N,N-dimethylthiocar- bamoyl chloride (DMTC) to form an O-(acylaryl) N,N-di(organo)thiocarbamate, e.g., O-(4'-acetophenyl) N,N-dimethylthiocarbamate, and pyrolytically rearranging the latter compound. The acylthiophenol may be produced by hydrolyzing the S-(acylaryl) N,N-di(organo)thiocarbamate.
    本发明提供了一种制备 N-酰基氨基苯硫酚,例如 N-乙酰基对氨基苯硫酚,或氨基苯硫酚,例如对氨基苯硫酚的方法,该方法通过使某些含硫酮中的任何一种,即 S-(酰基)-N,N-二(有机)硫代氨基甲酸酯,例如 S-(4'-乙酰苯基)-N,N-二甲基硫代氨基甲酸酯反应来制备、S-(酰基)N,N-二(有机)硫代氨基甲酸酯,如 S-(4'-乙酰苯基)-N,N-二甲基硫代氨基甲酸酯,酰基苯硫酚酰基酯,如 4-乙酰苯硫酚乙酸酯,或游离酰基苯硫酚,如 4-乙酰苯硫酚乙酸酯、将 4-乙酰苯硫酚与羟胺或羟胺盐一起形成酮的肟,在催化剂存在下使肟进行贝克曼重排,形成 S-(N-乙酰基-氨基芳基) N,N-二(有机)硫代氨基甲酸酯,例如S-(N-乙酰基-副氨基苯基) N,N-二甲基硫代氨基甲酸酯、N,S-二乙酰基氨基苯硫酚,如 N,S-二乙酰基-副氨基苯硫酚,或 N-酰基氨基苯硫酚,如 N-乙酰基-副氨基苯硫酚。S-(N-酰基-氨基芳基)N,N-二(有机)硫代氨基甲酸酯可水解为 N-酰基氨基苯硫酚或氨基苯硫酚。S-(酰基)N,N-二(有机)硫代氨基甲酸酯可通过羟基芳香酮(如 4-羟基苯乙酮 (4-HAP))与 N,N-二(有机)硫代氨基甲酰卤(如 N,N-二甲基硫代氨基甲酰卤)反应制得、N,N-二甲基硫代氨基甲酰氯(DMTC)形成 O-(酰基)N,N-二(有机)硫代氨基甲酸 酯,如 O-(4'-乙酰苯基)N,N-二甲基硫代氨基甲酸酯,并对后一种化合物进行热解重排。酰基苯硫酚可通过水解 S-(酰基)N,N-二(有机)硫代氨基甲酸酯而制得。
  • ASLAM, MOHAMMAD;DAVENPORT, KENNETH G., SYNTH. COMMUN., 17,(1987) N 5, 1761-1768
    作者:ASLAM, MOHAMMAD、DAVENPORT, KENNETH G.
    DOI:——
    日期:——
  • US5157142A
    申请人:——
    公开号:US5157142A
    公开(公告)日:1992-10-20
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