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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
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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
28598-82-5
合成路线
(共 5 条)
28598-82-5
→
反应条件
103904-73-0
反应条件
1.1: BuLi; HMPA / hexane; tetrahydrofuran / 0.5 h / 0 °C 1.2: 89.4 percent / hexane; tetrahydrofuran / 1 h / 0 °C 2.1: 77.3 percent / hydroquinone; aq. H3PO4 / dioxane / 4.5 h / 100 °C 3.1: 60.8 percent / methanol / 1.5 h / 20 °C 4.1: 79.5 percent / Ag2O / CH2Cl2 / 24 h / 20 °C 5.1: 95.4 percent / NaI / acetone / 24 h / Heating 6.1: 82.4 percent / NaHCO3; DMSO / 11 h / 90 °C 7.1: BuLi / hexane; tetrahydrofuran / 1 h / 20 °C 7.2: 69.3 percent / tetrahydrofuran / 0.5 h / 20 °C 8.1: 75 percent / BBr3 / CH2Cl2 / 1 h / 20 °C 9.1: 88.5 percent / 10 percent NaOH / ethanol / 6 h / Heating View Scheme
参考文献
Satoh; Takeuchi; Nishimura; Ohta; Tobinaga
Chemical and Pharmaceutical Bulletin, 2001 , vol. 49, # 1 p. 18 - 22
28598-82-5
→
反应条件
16725-53-4
顺-9-十四碳烯乙酸酯
反应条件
1: Na, liq. NH3 / diethyl ether 2: NaNH2 / diethyl ether 3: H2 / Lindlar catalyst / methanol 4: NaI / dimethylsulfoxide View Scheme
参考文献
Kovaleva,A.S. et al.
Journal of Organic Chemistry USSR (English Translation), 1972 , vol. 8, p. 2523 - 2527
Zhurnal Organicheskoi Khimii, 1972 , vol. 8, p. 2474 - 2479
28598-82-5
→
反应条件
22910-60-7
银杏酸
反应条件
1.1: BuLi; HMPA / hexane; tetrahydrofuran / 0.5 h / 0 °C 1.2: 89.4 percent / hexane; tetrahydrofuran / 1 h / 0 °C 2.1: 77.3 percent / hydroquinone; aq. H3PO4 / dioxane / 4.5 h / 100 °C 3.1: 60.8 percent / methanol / 1.5 h / 20 °C 4.1: 79.5 percent / Ag2O / CH2Cl2 / 24 h / 20 °C 5.1: 95.4 percent / NaI / acetone / 24 h / Heating 6.1: 82.4 percent / NaHCO3; DMSO / 11 h / 90 °C 7.1: BuLi / tetrahydrofuran / 1 h / 20 °C 7.2: 76.4 percent / tetrahydrofuran / 0.5 h / 0 °C 8.1: 66.9 percent / BBr3 / CH2Cl2 / 0.25 h / 20 °C 9.1: 92.9 percent / 10 percent NaOH / ethanol / 2 h / Heating View Scheme
参考文献
Satoh; Takeuchi; Nishimura; Ohta; Tobinaga
Chemical and Pharmaceutical Bulletin, 2001 , vol. 49, # 1 p. 18 - 22
28598-82-5
→
反应条件
103904-74-1
反应条件
1.1: BuLi; HMPA / hexane; tetrahydrofuran / 0.5 h / 0 °C 1.2: 89.4 percent / hexane; tetrahydrofuran / 1 h / 0 °C 2.1: 77.3 percent / hydroquinone; aq. H3PO4 / dioxane / 4.5 h / 100 °C 3.1: 60.8 percent / methanol / 1.5 h / 20 °C 4.1: 79.5 percent / Ag2O / CH2Cl2 / 24 h / 20 °C 5.1: 95.4 percent / NaI / acetone / 24 h / Heating 6.1: 82.4 percent / NaHCO3; DMSO / 11 h / 90 °C 7.1: BuLi / hexane; tetrahydrofuran / 1 h / 20 °C 7.2: 66.7 percent / tetrahydrofuran / 0.5 h / 20 °C 8.1: 97.1 percent / BBr3 / CH2Cl2 / 1 h / 20 °C 9.1: 86.5 percent / 10 percent NaOH / ethanol / 6 h / Heating View Scheme
参考文献
Satoh; Takeuchi; Nishimura; Ohta; Tobinaga
Chemical and Pharmaceutical Bulletin, 2001 , vol. 49, # 1 p. 18 - 22
28598-82-5
→
反应条件
42513-41-7
反应条件
1: Na, liq. NH3 / diethyl ether 2: NaNH2 / diethyl ether 3: H2 / Lindlar catalyst / methanol View Scheme
参考文献
Kovaleva,A.S. et al.
Journal of Organic Chemistry USSR (English Translation), 1972 , vol. 8, p. 2523 - 2527
Zhurnal Organicheskoi Khimii, 1972 , vol. 8, p. 2474 - 2479