- 英文名称2,3,6-Trifluoropyridine
- 中文名称2,3,6-三氟吡啶
- IUPAC名称2,3,6-trifluoropyridine
- 其它别名2,3,6-Trifluoropyridine; Pyridine, 2,3,6-Trifluoro-; 2,3,6-Trifluoro-Pyridine; 2,3,6-Tris(Fluoranyl)Pyridine; Hrliangjwpjfkw-Uhfffaoysa-N
- CAS编号3512-18-3
- MFCD编号:MFCD03001158
- EINECS号:680-721-0
- 分子式:C5H2F3N
- 分子量:133.07
- 产品CID: 1356988
- 产品分类有机原料→分子砌块→芳杂环类化合物→吡啶类化合物
相似化合物
2875-18-5 76469-41-5 1513-66-2欧盟法规
ECHA物质C&L通报上下游产品
CAS号2879-42-7 3-氯-2,5,6-三氟吡啶 | CAS号2875-18-5 2,3,5,6-四氟吡啶 | CAS号849937-92-4 2,3,6-trifluoro... | CAS号1735-84-8 3-氯-2,4,5,6-四氟吡啶 | CAS号110-86-1 吡啶 | CAS号3512-13-8 2,3,4,6-四氟吡啶 | CAS号1333-74-0 氢 | CAS号121-46-0 2,5-降冰片二烯 | CAS号75995-67-4 3,5,6-trifluoro... | CAS号1257071-45-6 6-溴-2,3-二氟吡啶 | CAS号905587-08-8 2,3,6-三氟-5-硝基吡啶合成工艺路线路线简述
- 700-16-3 + 99476-19-4 = 3512-18-3 + 76469-41-5 + 71902-33-5 + 372-47-4 + 84476-99-3
反应条件:1.1 Solvents: Toluene; 3 D,Rt2.1 Reagents: Triethylsilane Catalysts: Di-μ-Hydrobis[1,1′-(1,3-Propanediyl)Bis[1,1-Bis(1-Methylethyl)Phosphine-Kp]]Dirh... Solvents: Benzene-D6; 48 H,Rt -> 50 °C
标题:Catalytic Hydrodefluorination Of Fluoroaromatics With Silanes As Hydrogen Source At A Binuclear Rhodium Complex: Characterization Of Key Intermediates
作者:Zamostna,Lada; Et Al
参考文献:Journal Of Fluorine Chemistry 日期:2013 卷标:155 页码:132-142]
2875-18-5 = 3512-18-3 + 76469-41-5 + 71902-33-5 + 372-47-4 + 84476-99-3
反应条件:1.1 Reagents: Triethylsilane Catalysts: Di-μ-Hydrobis[1,1′-(1,3-Propanediyl)Bis[1,1-Bis(1-Methylethyl)Phosphine-Kp]]Dirh... Solvents: Benzene-D6; 48 H,Rt -> 50 °C
标题:Catalytic Hydrodefluorination Of Fluoroaromatics With Silanes As Hydrogen Source At A Binuclear Rhodium Complex: Characterization Of Key Intermediates
作者:Zamostna,Lada; Et Al
参考文献:Journal Of Fluorine Chemistry 日期:2013 卷标:155 页码:132-142]
700-16-3 = 3512-18-3 + 76469-41-5 + 71902-33-5 + 372-47-4 + 84476-99-3
反应条件:1.1 Reagents: Triethylsilane Catalysts: Di-μ-Hydrobis[1,1′-(1,3-Propanediyl)Bis[1,1-Bis(1-Methylethyl)Phosphine-Kp]]Dirh... Solvents: Benzene-D6; 48 H,Rt -> 50 °C2.1 Reagents: Triethylsilane Catalysts: Di-μ-Hydrobis[1,1′-(1,3-Propanediyl)Bis[1,1-Bis(1-Methylethyl)Phosphine-Kp]]Dirh... Solvents: Benzene-D6; 48 H,Rt -> 50 °C
标题:Catalytic Hydrodefluorination Of Fluoroaromatics With Silanes As Hydrogen Source At A Binuclear Rhodium Complex: Characterization Of Key Intermediates
作者:Zamostna,Lada; Et Al
参考文献:Journal Of Fluorine Chemistry 日期:2013 卷标:155 页码:132-142]
6485-79-6 = 3512-18-3 + 76469-41-5 + 71902-33-5 + 372-47-4 + 84476-99-3
反应条件:1.1 Solvents: Toluene-D8; 2 H,Rt2.1 Solvents: Toluene; 3 D,Rt3.1 Reagents: Triethylsilane Catalysts: Di-μ-Hydrobis[1,1′-(1,3-Propanediyl)Bis[1,1-Bis(1-Methylethyl)Phosphine-Kp]]Dirh... Solvents: Benzene-D6; 48 H,Rt -> 50 °C
标题:Catalytic Hydrodefluorination Of Fluoroaromatics With Silanes As Hydrogen Source At A Binuclear Rhodium Complex: Characterization Of Key Intermediates
作者:Zamostna,Lada; Et Al
参考文献:Journal Of Fluorine Chemistry 日期:2013 卷标:155 页码:132-142]
= 3512-18-3 + 76469-41-5 + 71902-33-5 + 372-47-4 + 84476-99-3
反应条件:1.1 Solvents: Toluene-D8; 8 H,Rt -> 50 °C2.1 Solvents: Toluene; 3 D,Rt3.1 Reagents: Triethylsilane Catalysts: Di-μ-Hydrobis[1,1′-(1,3-Propanediyl)Bis[1,1-Bis(1-Methylethyl)Phosphine-Kp]]Dirh... Solvents: Benzene-D6; 48 H,Rt -> 50 °C
标题:Catalytic Hydrodefluorination Of Fluoroaromatics With Silanes As Hydrogen Source At A Binuclear Rhodium Complex: Characterization Of Key Intermediates
作者:Zamostna,Lada; Et Al
参考文献:Journal Of Fluorine Chemistry 日期:2013 卷标:155 页码:132-142]
= 3512-18-3 + 76469-41-5 + 71902-33-5 + 372-47-4 + 84476-99-3
反应条件:1.1 Solvents: Toluene-D8; 8 H,Rt -> 50 °C2.1 Solvents: Toluene; 3 D,Rt3.1 Reagents: Triethylsilane Catalysts: Di-μ-Hydrobis[1,1′-(1,3-Propanediyl)Bis[1,1-Bis(1-Methylethyl)Phosphine-Kp]]Dirh... Solvents: Benzene-D6; 48 H,Rt -> 50 °C
标题:Catalytic Hydrodefluorination Of Fluoroaromatics With Silanes As Hydrogen Source At A Binuclear Rhodium Complex: Characterization Of Key Intermediates
作者:Zamostna,Lada; Et Al
参考文献:Journal Of Fluorine Chemistry 日期:2013 卷标:155 页码:132-142]
617-86-7 = 3512-18-3 + 76469-41-5 + 71902-33-5 + 372-47-4 + 84476-99-3
反应条件:1.1 Solvents: Toluene-D8; -30 °C; 20 H,-15 °C2.1 Solvents: Toluene-D8; 2 H,Rt3.1 Solvents: Toluene; 3 D,Rt4.1 Reagents: Triethylsilane Catalysts: Di-μ-Hydrobis[1,1′-(1,3-Propanediyl)Bis[1,1-Bis(1-Methylethyl)Phosphine-Kp]]Dirh... Solvents: Benzene-D6; 48 H,Rt -> 50 °C
标题:Catalytic Hydrodefluorination Of Fluoroaromatics With Silanes As Hydrogen Source At A Binuclear Rhodium Complex: Characterization Of Key Intermediates
作者:Zamostna,Lada; Et Al
参考文献:Journal Of Fluorine Chemistry 日期:2013 卷标:155 页码:132-142]
6485-79-6 = 3512-18-3 + 76469-41-5 + 71902-33-5 + 372-47-4 + 84476-99-3
反应条件:1.1 Solvents: Toluene-D8; -30 °C; 20 H,-15 °C2.1 Solvents: Toluene-D8; 8 H,Rt -> 50 °C3.1 Solvents: Toluene; 3 D,Rt4.1 Reagents: Triethylsilane Catalysts: Di-μ-Hydrobis[1,1′-(1,3-Propanediyl)Bis[1,1-Bis(1-Methylethyl)Phosphine-Kp]]Dirh... Solvents: Benzene-D6; 48 H,Rt -> 50 °C
标题:Catalytic Hydrodefluorination Of Fluoroaromatics With Silanes As Hydrogen Source At A Binuclear Rhodium Complex: Characterization Of Key Intermediates
作者:Zamostna,Lada; Et Al
参考文献:Journal Of Fluorine Chemistry 日期:2013 卷标:155 页码:132-142
3-氯-2,4,5,6-四氟吡啶置于palladium On Activated Charcoal Sodium Tetrahydroborate,甲酸铵体系中,用 辛醇,乙醇 用作溶剂,化学反应生成2,3,6-三氟吡啶
参考文献:从聚卤代吡啶中除去氟并将氟引入到聚卤代吡啶中:亲核性戊烯取代反应.
标题:从聚卤代吡啶中除去氟并将氟引入到聚卤代吡啶中:亲核性戊烯取代反应.
摘要:从六个工业上可获得的氟化吡啶开始,开发了一种方便的途径来获取所有三个四氟吡啶(2-4),所有六个三氟吡啶(5-10)和五个非商业性二氟吡啶(11-14和16).用于从多氟吡啶中选择性除去氟的方法是通过金属或复合氢化物进行还原,并用肼进行位点选择性置换,然后进行脱氢-脱重氮或脱氢氯化-脱重氮.为了引入额外的氟原子,在进行氯/氟置换过程之前,将合适的前体金属化和氯化.
Doi:10.1002/chem.200400837
专利信息
专利号:EP-3686190-A1
优先权日:2013-07-11
标 题 :Synthesis of therapeutically active compounds