1-phenoxy-3-acetylsulfanylpropane | 60197-89-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 1-phenoxy-3-acetylsulfanylpropane
• 英文别名: Thioacetic Acid S-(3-phenoxypropyl)ester；S-(3-phenoxypropyl) ethanethioate
• CAS: 60197-89-9
• 化学式: C₁₁H₁₄O₂S
• 分子量: 210.297
• InChiKey: BFGHIIOMOUYXHC-UHFFFAOYSA-N

物化性质

• 沸点：
  320.8±25.0 °C(Predicted)
• 密度：
  1.103±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  14
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  51.6
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  1-phenoxy-3-acetylsulfanylpropane 在 potassium thioacetate 作用下， 以 DMF (N,N-dimethyl-formamide) 为溶剂， 反应 18.0h， 生成 methyl 4-(acetylsulfanylmethyl)tetrahydropyran-4-carboxylate
  参考文献：
  名称：

  HYDROXAMIC AND CARBOXYLIC ACID DERIVATIVES

  摘要：

  具有治疗效用的化合物的公式为(I)B—X—(CH2)n—CR2R3—CR4R5—COY  (I)，其中n为0-1；X为S(O)0-2，Y为OR1或NHOH；R2和R4独立地为H或从C1-6烷基、C2-6烯基、芳基、C1-6烷基芳基、杂芳基、C1-6烷基杂芳基、杂环烷基、C1-6烷基杂环烷基、环烷基和C1-6烷基环烷基中选择的（可选地用R10取代的）基团；R1、R3和R5独立地为H或C1-6烷基；但不得超过两个R2、R3、R4和R5为H；或CR2R3、CR4R5和CR2—CR4中的任何一个为杂环烷基或杂环烷基环，可选地用R10取代，或从C1-6烷基、芳基、C1-6烷基芳基、杂芳基和C1-6烷基杂芳基中选择的（可选地用R10取代的）基团；B为通过碳与X相连的杂环烷基（可选地用R6或R7取代），或C1-6烷基杂环烷基（可选地用R6或R7取代），或从C1-8烷基、C2-6烯基和C2-6炔基中选择的（用R6取代的）基团；R6为N(R7)2、OR7、COR7、C(=NOR9)R7、NR7R8、S(O)0-2R9或SO2N(R7)2；R7为H或从C1-6烷基、芳基、C1-6烷基芳基、杂芳基、C1-6烷基杂芳基、环烷基、C1-6烷基环烷基、杂环烷基和C1-6烷基杂环烷基中选择的基团，其中所述基团可选地用R9、COR9、SO0-2R9、CO2R9、OR9、CONR1R9、NR1R9、卤素、CN、SO2NR1R9或NO2取代，对于每种情况的N(R7)2，R7基团相同或不同，或N(R7)2为可选地用R9、COR9、SO0-2R9、CO2R9、OR9、CONR1R9、NR1R9、卤素、CN、SO2NR1R9或NO2取代的杂环烷基；R8为COR7、CON(R7)2、CO2R9或SO2R9；R9为C1-6烷基、芳基、C1-6烷基芳基、杂芳基或C1-6烷基杂芳基；R10为OR7、COR7、CO2R1、CON(R7)2、NR7R8、S(O)0-2R9、SO2N(R7)2、CN、卤素或环亚咪唑基（可选地用R1取代）；及其盐、溶剂化合物、水合物、N-氧化物、保护氨基、保护羧基和保护羟胺衍生物。

  公开号：

  US20030236416A1
• 作为产物：
  描述：

  3-苯氧基溴丙烷 在 溴 、 溶剂黄146 作用下， 以 四氢呋喃 为溶剂， 反应 16.0h， 生成 1-phenoxy-3-acetylsulfanylpropane
  参考文献：
  名称：

  Bromine catalyzed conversion of S-tert-butyl groups into versatile and, for self-assembly processes accessible, acetyl-protected thiols

  摘要：

  在乙酰氯和乙酸存在的情况下，通过催化溴的用量，将叔丁基保护基团简便高效地转化为硫醇的乙酰基保护基团。这种相当温和的反应条件对于硫官能化目标结构的新保护基策略具有特别重要的意义。

  DOI：

  10.1039/b408677e

文献信息

• Hydroxamic and carboxylic acid derivatives
  申请人：Darwin Discovery Ltd.

  公开号：US06680338B2

  公开（公告）日：2004-01-20

  Compounds having therapeutic utility are of formula (I) B—X—(CH2)n—CR2R3—CR4R5—COY  (I) wherein n=0-1; X is S(O)0-2; Y is OR1 or NHOH; R2 and R4 are independently H or a group (optionally substituted with R10) selected from C1-6 alkyl, C2-6 alkenyl, aryl, C1-6 alkyl-aryl, heteroaryl, C1-6 alkyl-heteroaryl, heterocycloalkyl, C1-6 alkyl-heterocycloalkyl, cycloalkyl and C1-6 alkyl-cycloalkyl; and R1, R3 and R5 are independently H or C1-6 alkyl, provided that not more than two of R2, R3, R4 and R5 are H; or any of CR2R3, CR4R5 and CR2—CR4 is a cycloalkyl or heterocycloalkyl ring optionally substituted with R10 or a group (optionally substituted with R10) selected from C1-6 alkyl, aryl, C1-6 alkyl-aryl, heteroaryl and C1-6 alkyl-heteroaryl; B is heterocycloalkyl (optionally substituted by R6 or R7) bonded through carbon to X, or C1-6 alkyl-heterocycloalkyl (optionally substituted with R6 or R7), or a group (substituted with R6) selected from C1-8 alkyl, C2-6 alkenyl and C2-6 alkynyl; R6 is N(R7)2, OR7, COR7, C(═NOR9)R7, NR7R8, S(O)0-2R9 or SO2N(R7)2; R7 is H or a group selected from C1-6 alkyl, aryl, C1-6 alkyl-aryl, heteroaryl, C1-6 alkyl-heteroaryl, cycloalkyl, C1-6 alkyl-cycloalkyl, heterocycloalkyl and C1-6 alkyl-heterocycloalkyl, wherein said group is optionally substituted with R9, COR9, SO0-2R9, CO2R9, OR9, CONR1R9, NR1R9, halogen, CN, SO2NR1R9 or NO2, and for each case of N(R7)2 the R7 groups are the same or different or N(R7)2 is heterocycloalkyl optionally substituted with R9, COR9, SO0-2R9, CO2R9, OR9, CONR1R9, NR1R9, NR1R9 halogen, CN, SO2NR1R9 or NO2, R8 is COR7, CON(R7)2, CO2R9 or SO2R9; R9 is C1-6 alkyl, aryl, C1-6 alkyl-aryl, heteroaryl or C1-6 alkyl-heteroaryl; and R10 is OR7, COR7, CO2R1, CON(R7)2, NR7R8, S(O)0-2R9, SO2N(R7)2, CN, halogen or cycloimidyl (optionally substituted with R1); and the salts, solvates, hydrates, N-oxides, protected amino, protected carboxy and protected hydroxamic acid derivatives thereof.

  具有治疗效用的化合物的公式为(I)B—X—(CH2)n—CR2R3—CR4R5—COY  (I)，其中n为0-1；X为S(O)0-2；Y为OR1或NHOH；R2和R4独立地为H或从C1-6烷基、C2-6烯基、芳基、C1-6烷基-芳基、杂芳基、C1-6烷基-杂芳基、杂环烷基、C1-6烷基-杂环烷基、环烷基和C1-6烷基-环烷基中选取的（可选地取代R10的）基团；R1、R3和R5独立地为H或C1-6烷基，前提是R2、R3、R4和R5中不超过两个为H；或CR2R3、CR4R5和CR2—CR4中的任何一个为杂环烷基或环状杂环烷基，可选地取代R10或从C1-6烷基、芳基、C1-6烷基-芳基、杂芳基和C1-6烷基-杂芳基中选取的（可选地取代R10的）基团；B为通过碳与X相连的杂环烷基（可选地取代R6或R7），或C1-6烷基-杂环烷基（可选地取代R6或R7），或从C1-8烷基、C2-6烯基和C2-6炔基中选取的（取代R6的）基团；R6为N（R7）2、OR7、COR7、C(═NOR9)R7、NR7R8、S(O)0-2R9或SO2N（R7）2；R7为H或从C1-6烷基、芳基、C1-6烷基-芳基、杂芳基、环烷基、C1-6烷基-环烷基、杂环烷基和C1-6烷基-杂环烷基中选取的基团，其中所述基团可选地取代R9、COR9、SO0-2R9、CO2R9、OR9、CONR1R9、NR1R9、卤素、CN、SO2NR1R9或NO2，对于每种N（R7）2的情况，R7基团相同或不同，或N（R7）2为可选地取代R9、COR9、SO0-2R9、CO2R9、OR9、CONR1R9、NR1R9、NR1R9卤素、CN、SO2NR1R9或NO2的杂环烷基；R8为COR7、CON（R7）2、CO2R9或SO2R9；R9为C1-6烷基、芳基、C1-6烷基-芳基、杂芳基或C1-6烷基-杂芳基；R10为OR7、COR7、CO2R1、CON（R7）2、NR7R8、S(O)0-2R9、SO2N（R7）2、CN、卤素或环戊亚胺基（可选地取代R1）；以及其盐、溶剂化物、水合物、N-氧化物、保护氨基、保护羧基和保护羟胺酸衍生物。
• US6680338B2
  申请人：——

  公开号：US6680338B2

  公开（公告）日：2004-01-20
• HYDROXAMIC AND CARBOXYLIC ACID DERIVATIVES
  申请人：——

  公开号：US20030236416A1

  公开（公告）日：2003-12-25

  Compounds having therapeutic utility are of formula (I) B—X—(CH 2 ) n —CR 2 R 3 —CR 4 R 5 —COY  (I) wherein n = 0 - 1; X is S(O) 0-2 , Y is OR 1 or NHOH; R 2 and R 4 are independently H or a group (optionally substituted with R 10 ) selected from C 1-6 alkyl, C 2-6 alkenyl, aryl, C 1-6 alkyl-aryl, heteroaryl, C 1-6 alkyl-heteroaryl, heterocycloalkyl, C 1-6 alkyl-heterocycloalkyl, cycloalkyl and C 1-6 alkyl-cycloalkyl; and R 1 , R 3 and R 5 are independently H or C 1-6 alkyl; provided that not more than two of R 2 , R 3 , R 4 and R 5 are H; or any of CR 2 R 3 , CR 4 R 5 and CR 2 —CR 4 is a cycloalkyl or heterocycloalkyl ring optionally substituted with R 10 or a group (optionally substituted with R 10 ) selected from C 1-6 alkyl, aryl, C 1-6 alkyl-aryl, heteroaryl and C 1-6 alkyl-heteroaryl; B is heterocycloalkyl (optionally substituted by R 6 or R 7 ) bonded through carbon to X, or C 1-6 alkyl-heterocycloalkyl (optionally substituted with R 6 or R 7 ), or a group (substituted with R 6 ) selected from C 1-8 alkyl, C 2-6 alkenyl and C 2-6 alkynyl; R 6 is N(R 7 ) 2 , OR 7 , COR 7 , C(=NOR 9 )R 7 , NR 7 R 8 , S(O) 0-2 R 9 or SO 2 N(R 7 ) 2 ; R 7 is H or a group selected from C 1-6 alkyl, aryl, C 1-6 alkyl-aryl, heteroaryl, C 1-6 alkyl-heteroaryl, cycloalkyl, C 1-6 alkyl-cycloalkyl, heterocycloalkyl and C 1-6 alkyl-heterocycloalkyl, wherein said group is optionally substituted with R 9 , COR 9 , SO 0-2 R 9 , CO 2 R 9 , OR 9 , CONR 1 R 9 , NR 1 R 9 , halogen, CN, SO 2 NR 1 R 9 or NO 2 , and for each case of N(R 7 ) 2 the R 7 groups are the same or different or N(R 7 ) 2 is heterocycloalkyl optionally substituted with R 9 , COR 9 , SO 0-2 R 9 , CO 2 R 9 , OR 9 , CONR 1 R 9 , NR 1 R 9 , halogen, CN, SO 2 NR 1 R 9 or NO 2 ; R 8 is COR 7 , CON(R 7 ) 2 , CO 2 R 9 or SO 2 R 9 ; R 9 is C 1-6 alkyl, aryl, C 1-6 alkyl-aryl, heteroaryl or C 1-6 alkyl-heteroaryl; and R 10 is OR 7 , COR 7 , CO 2 R 1 , CON(R 7 ) 2 , NR 7 R 8 , S(O) 0-2 R 9 , SO 2 N(R 7 ) 2 , CN, halogen or cycloimidyl (optionally substituted with R 1 ); and the salts, solvates, hydrates, N-oxides, protected amino, protected carboxy and protected hydroxamic acid derivatives thereof.

  具有治疗效用的化合物的公式为(I)B—X—(CH2)n—CR2R3—CR4R5—COY  (I)，其中n为0-1；X为S(O)0-2，Y为OR1或NHOH；R2和R4独立地为H或从C1-6烷基、C2-6烯基、芳基、C1-6烷基芳基、杂芳基、C1-6烷基杂芳基、杂环烷基、C1-6烷基杂环烷基、环烷基和C1-6烷基环烷基中选择的（可选地用R10取代的）基团；R1、R3和R5独立地为H或C1-6烷基；但不得超过两个R2、R3、R4和R5为H；或CR2R3、CR4R5和CR2—CR4中的任何一个为杂环烷基或杂环烷基环，可选地用R10取代，或从C1-6烷基、芳基、C1-6烷基芳基、杂芳基和C1-6烷基杂芳基中选择的（可选地用R10取代的）基团；B为通过碳与X相连的杂环烷基（可选地用R6或R7取代），或C1-6烷基杂环烷基（可选地用R6或R7取代），或从C1-8烷基、C2-6烯基和C2-6炔基中选择的（用R6取代的）基团；R6为N(R7)2、OR7、COR7、C(=NOR9)R7、NR7R8、S(O)0-2R9或SO2N(R7)2；R7为H或从C1-6烷基、芳基、C1-6烷基芳基、杂芳基、C1-6烷基杂芳基、环烷基、C1-6烷基环烷基、杂环烷基和C1-6烷基杂环烷基中选择的基团，其中所述基团可选地用R9、COR9、SO0-2R9、CO2R9、OR9、CONR1R9、NR1R9、卤素、CN、SO2NR1R9或NO2取代，对于每种情况的N(R7)2，R7基团相同或不同，或N(R7)2为可选地用R9、COR9、SO0-2R9、CO2R9、OR9、CONR1R9、NR1R9、卤素、CN、SO2NR1R9或NO2取代的杂环烷基；R8为COR7、CON(R7)2、CO2R9或SO2R9；R9为C1-6烷基、芳基、C1-6烷基芳基、杂芳基或C1-6烷基杂芳基；R10为OR7、COR7、CO2R1、CON(R7)2、NR7R8、S(O)0-2R9、SO2N(R7)2、CN、卤素或环亚咪唑基（可选地用R1取代）；及其盐、溶剂化合物、水合物、N-氧化物、保护氨基、保护羧基和保护羟胺衍生物。
• Bromine catalyzed conversion of S-tert-butyl groups into versatile and, for self-assembly processes accessible, acetyl-protected thiols
  作者：Alfred Błaszczyk、Mark Elbing、Marcel Mayor

  DOI：10.1039/b408677e

  日期：——

  The facile and efficient conversion of a tert-butyl protecting group to an acetyl protecting group for thiols by catalytic amounts of bromine in acetyl chloride and the presence of acetic acid has been developed. The fairly mild reaction conditions are of particular interest for new protecting group strategies for sulfur functionalised target structures.

  在乙酰氯和乙酸存在的情况下，通过催化溴的用量，将叔丁基保护基团简便高效地转化为硫醇的乙酰基保护基团。这种相当温和的反应条件对于硫官能化目标结构的新保护基策略具有特别重要的意义。