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结构式
乙二醇
甲醛
63148-62-9
MDI
丁酮
二甲基亚砜
碳酸氢钠
471-34-1
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乙二醇
甲醛
63148-62-9
MDI
丁酮
二甲基亚砜
碳酸氢钠
471-34-1
1-辛炔
合成路线
(共 595 条)
629-05-0
1-辛炔
→
反应条件
31283-43-9
2-氯-1-辛烯
+
1119-89-7
反应条件
hydrogenchloride; anhydrous iron chloride; air; 1,2-dichloro-ethane in water T=75°C; 72 h;
参考文献
Wu, Xiao-Feng; Bezier, David; Darcel, Christophe
Advanced Synthesis and Catalysis, 2009 , vol. 351, # 3 p. 367 - 370
629-05-0
1-辛炔
+
79-04-9
一氯代乙酰氯
→
反应条件
31283-43-9
2-氯-1-辛烯
反应条件
[rhodium(I)(carbonyl)2(acetylacetonate)]; triphenylphosphine in toluene T=110°C; 14 h; Inert atmosphere;
参考文献
Kashiwabara, Taigo; Fuse, Kouichiro; Hua, Ruimao; Tanaka, Masato
Organic Letters, 2008 , vol. 10, # 23 p. 5469 - 5472
629-05-0
1-辛炔
+
79-04-9
一氯代乙酰氯
→
反应条件
31283-43-9
2-氯-1-辛烯
+
1047647-18-6
+
1047647-19-7
反应条件
[rhodium(I)(carbonyl)2(acetylacetonate)]; triphenyl-arsane in toluene T=110°C; 14 h; Inert atmosphere;
参考文献
Kashiwabara, Taigo; Fuse, Kouichiro; Hua, Ruimao; Tanaka, Masato
Organic Letters, 2008 , vol. 10, # 23 p. 5469 - 5472
629-05-0
1-辛炔
→
反应条件
33128-27-7
反应条件
oxygen; ammonium chloride; copper(l) chloride Reagens 4: wss.-alkoh.HCl;
参考文献
Black; Weedon
Journal of the Chemical Society, 1953 , p. 1785,1791
629-05-0
1-辛炔
→
反应条件
3158-56-3
5-十五烷间苯二酚
反应条件
1.1: n-butyllithium / tetrahydrofuran / -78 - 20 °C 1.2: 30 h / Reflux 2.1: quinoline; Lindlar's catalyst; hydrogen / cyclohexane / 4 h 3.1: palladium 10 on activated carbon; hydrogen / tetrahydrofuran / 18 h 4.1: methyl-magnesium iodide / tetrahydrofuran; diethyl ether / 0 - 170 °C / Inert atmosphere View Scheme
参考文献
Tanaka, Ayano; Arai, Yasuhiro; Kim, Su-Nam; Ham, Jungyeob; Usuki, Toyonobu
Journal of Asian Natural Products Research, 2011 , vol. 13, # 4 p. 290 - 296
629-05-0
1-辛炔
+
106-95-6
3-溴丙烯
→
反应条件
31508-11-9
反应条件
copper(l) iodide; ethylmagnesium bromide in diethyl ether T=-75°C;
参考文献
Bosshardt, Herbert; Schlosser, Manfred
Helvetica Chimica Acta, 1980 , vol. 63, # 8 p. 2393 - 2403
629-05-0
1-辛炔
+
98747-02-5
+
106-95-6
3-溴丙烯
→
反应条件
31508-11-9
反应条件
1: anhydrous 1-octyne; allyl bromide in tetrahydrofuran T=20°C; 0.5 h; 2: oct-1-en-2-yl trifluoromethanesulfonate With Co(acetylacetonate)3 in tetrahydrofuran T=20°C; 2 h; Further stages.;
参考文献
Shirakawa, Eiji; Sato, Takahiro; Imazaki, Yusuke; Kimura, Takahiro; Hayashi, Tamio
Chemical Communications, 2007 , # 43 p. 4513 - 4515
629-05-0
1-辛炔
+
1745-31-9
→
反应条件
31508-11-9
反应条件
Ni(P(OC3H7-i)3)4
参考文献
Catellani,M. et al.
Journal of Organometallic Chemistry, 1978 , vol. 146, p. C19 - C22
67-56-1
甲醇
+
629-05-0
1-辛炔
+
201230-82-2
→
反应条件
3618-40-4
反应条件
[Pd2(H2O)4(dppcb)](OTs)4; hydrogen in acetonitrile T=70°C; P=7757.43 Torr; 2 h; AutoclaveInert atmosphere; regioselective reaction;
参考文献
Oberhauser, Werner; Ienco, Andrea; Vizza, Francesco; Trettenbrein, Barbara; Oberhuber, Dennis; Strabler, Christof; Ortner, Teresa; Brueggeller, Peter
Organometallics, 2012 , vol. 31, # 13 p. 4832 - 4837
67-56-1
甲醇
+
629-05-0
1-辛炔
+
201230-82-2
→
反应条件
111-79-5
反式-2-壬烯酸甲酯
+
3618-40-4
反应条件
[Pd2(H2O)4(dppcb)](OTs)4; hydrogen in acetonitrile T=70°C; P=7757.43 Torr; 2 h; AutoclaveInert atmosphere; regioselective reaction;
参考文献
Oberhauser, Werner; Ienco, Andrea; Vizza, Francesco; Trettenbrein, Barbara; Oberhuber, Dennis; Strabler, Christof; Ortner, Teresa; Brueggeller, Peter
Organometallics, 2012 , vol. 31, # 13 p. 4832 - 4837
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