TW201930250A - 以配位體/鈀之比率進行二異丁烯之鈀催化羥基羰基化的方法 - Google Patents
以配位體/鈀之比率進行二異丁烯之鈀催化羥基羰基化的方法 Download PDFInfo
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Abstract
以配位體/鈀之比率進行二異丁烯之鈀催化羥基羰基化的方法。
Description
本發明係關於以配位體/鈀之比率進行二異丁烯之鈀催化羥基羰基化的方法。
包括丙酸、己二酸以及脂肪酸的羧酸用於製備聚合物、藥物、溶劑和食品添加劑。產生羧酸的途徑通常包括烴、醇或醛的氧化,經由臭氧分解的烯烴的氧化裂解,甘油三酯、腈、酯或醯胺的水解,格氏試劑(Grignard)或有機鋰試劑的羧化,以及鹵化和隨後鹵代反應中的甲基酮的水解。
烯烴的羥基羧化是用於獲得羧酸的非常有前途以及環境友好的方法。經由甲醇的羰基化產生乙酸,其用碘化物進行。在Koch反應中,向烯烴中加入水和一氧化碳是經由強鹼催化的。該方法對於形成二級和三級碳陽離子的烯烴是有效的,例如,異丁烯至新戊酸。通過同時向烯烴/炔烴中加入CO和H2 O而發生的羥基羧化提供合成羧酸的直接且方便的方法。
烯烴的羥基羧化是用於獲得羧酸的非常有前途以及環境友好的方法。經由甲醇的羰基化產生乙酸,其用碘化物進行。在Koch反應中,向烯烴中加入水和一氧化碳是經由強鹼催化的。該方法對於形成二級和三級碳陽離子的烯烴是有效的,例如,異丁烯至新戊酸。通過同時向烯烴/炔烴中加入CO和H2 O而發生的羥基羧化提供合成羧酸的直接且方便的方法。
本發明之目的係提供在二異丁烯(DIBN)之鈀催化羥基羰基化中的良好轉換方法。該反應必須在一個步驟中進行。
經由如申請專利範圍第1項所述之方法完成該目的。
方法,其包含以下步驟:
a) 加入二異丁烯,
b) 加入含有鈀的化合物,其中該鈀係具有能形成錯合物之能力,
c) 加入配位體L1:
其中該配位體L1係以每mole鈀加入1.0 mol 至2.0 mol之範圍的配位體L1的量,
d) 加入乙酸,
e) 在CO中進料,
f) 加熱該反應混合物以使該二異丁烯轉變為該化合物P1:
。
在該方法的一個變化形中,該化合物在方法步驟b)係選自於:PdCl2 、PdBr2 、Pd(acac)2 、Pd(dba)2 (dba=二苯乙烯基丙酮)、PdCl2 (CH3 CN)2 。
在該方法的一個變化形中,該方法步驟b)係Pd(acac)2 。
在該方法的一個變化形中,該配位體L1係以每mole鈀加入1.25 mol至1.75 mol之範圍的配位體L1的量。
在該方法的一個變化形中,在方法步驟f)中該反應混合物係加熱至80°C至160°C的範圍之溫度,較佳係在100°C至140°C的範圍之溫度。
在該方法的一個變化形中,在方法步驟e)中進料該CO以使該反應在10巴至40巴之範圍的CO壓力下進行,較佳係10巴至30巴之範圍。
在該方法的一個變化形中,該方法包含其他的方法步驟g):
g) 加入硫酸。
經由如申請專利範圍第1項所述之方法完成該目的。
方法,其包含以下步驟:
a) 加入二異丁烯,
b) 加入含有鈀的化合物,其中該鈀係具有能形成錯合物之能力,
c) 加入配位體L1:
其中該配位體L1係以每mole鈀加入1.0 mol 至2.0 mol之範圍的配位體L1的量,
d) 加入乙酸,
e) 在CO中進料,
f) 加熱該反應混合物以使該二異丁烯轉變為該化合物P1:
。
在該方法的一個變化形中,該化合物在方法步驟b)係選自於:PdCl2 、PdBr2 、Pd(acac)2 、Pd(dba)2 (dba=二苯乙烯基丙酮)、PdCl2 (CH3 CN)2 。
在該方法的一個變化形中,該方法步驟b)係Pd(acac)2 。
在該方法的一個變化形中,該配位體L1係以每mole鈀加入1.25 mol至1.75 mol之範圍的配位體L1的量。
在該方法的一個變化形中,在方法步驟f)中該反應混合物係加熱至80°C至160°C的範圍之溫度,較佳係在100°C至140°C的範圍之溫度。
在該方法的一個變化形中,在方法步驟e)中進料該CO以使該反應在10巴至40巴之範圍的CO壓力下進行,較佳係10巴至30巴之範圍。
在該方法的一個變化形中,該方法包含其他的方法步驟g):
g) 加入硫酸。
經由以下的工作實施例更詳細地闡述本發明。
在4 mL小燒瓶中加入[Pd(acac)2 ](1.75 mg, 0.25 mol%)、L1(4.44 mg, 0.375 mol%)、H2 SO4 (3.1 mg, 1.4 mol%)和已烘箱乾燥的攪拌棒。然後用隔膜(PTFE塗覆的苯乙烯-丁二烯橡膠)和酚醛樹脂蓋密封小燒瓶。將小燒瓶抽真空並用氬氣再填充三次。H2 O(0.29 ml)、乙酸(0.85 ml)以及二異丁烯(DIBN)(2.3 mmol)經由針筒加入至小燒瓶。將小燒瓶至於合金板上,在氬氣氛下將其轉移至Parr Instruments的4560系列高壓滅菌器(300 ml)中。用CO沖洗高壓滅菌器三次後,在室溫下CO的壓力增加到15巴,且接著以N2 將壓力增加到25巴。反應在120℃下進行3小時。在反應結束時,將高壓滅菌器冷卻至室溫並小心地解壓。然後加入異辛烷(100 µl)作為內部標準。經由GC分析測量轉化率。
以改變L1/Pd的比率重複上述實驗。維持所有其他的參數。
該結果整理如下表中。
*本發明方法
如實驗結果所示,該目的通過本發明的方法實現。
在4 mL小燒瓶中加入[Pd(acac)2 ](1.75 mg, 0.25 mol%)、L1(4.44 mg, 0.375 mol%)、H2 SO4 (3.1 mg, 1.4 mol%)和已烘箱乾燥的攪拌棒。然後用隔膜(PTFE塗覆的苯乙烯-丁二烯橡膠)和酚醛樹脂蓋密封小燒瓶。將小燒瓶抽真空並用氬氣再填充三次。H2 O(0.29 ml)、乙酸(0.85 ml)以及二異丁烯(DIBN)(2.3 mmol)經由針筒加入至小燒瓶。將小燒瓶至於合金板上,在氬氣氛下將其轉移至Parr Instruments的4560系列高壓滅菌器(300 ml)中。用CO沖洗高壓滅菌器三次後,在室溫下CO的壓力增加到15巴,且接著以N2 將壓力增加到25巴。反應在120℃下進行3小時。在反應結束時,將高壓滅菌器冷卻至室溫並小心地解壓。然後加入異辛烷(100 µl)作為內部標準。經由GC分析測量轉化率。
以改變L1/Pd的比率重複上述實驗。維持所有其他的參數。
該結果整理如下表中。
*本發明方法
如實驗結果所示,該目的通過本發明的方法實現。
Claims (6)
- 一種方法,其包含以下方法步驟: a) 加入二異丁烯, b) 加入含有鈀的化合物,其中該鈀係具有能形成錯合物之能力, c) 加入配位體L1 : 其中該配位體L1 係以每mole鈀加入1.0 mol 至2.0 mol之範圍的配位體L1 的量, d) 加入乙酸 e) 在CO中進料, f) 加熱該反應混合物以使該二異丁烯轉變為該化合物P1 :。
- 如申請專利範圍第1項所述之方法, 其中該化合物在方法步驟b)係選自於: PdCl2 、PdBr2 、Pd(acac)2 、Pd(dba)2 (dba=二苯乙烯基丙酮)、PdCl2 (CH3 CN)2 。
- 如申請專利範圍第1項至第2項中任一項所述之方法, 其中該配位體L1 係以每mole鈀加入1.25 mol至1.75 mol之範圍的配位體L1 的量。
- 如申請專利範圍第1項至第3項中任一項所述之方法, 其中在方法步驟f)中該反應混合物係加熱至80°C至160°C的範圍之溫度。
- 如申請專利範圍第1項至第4項中任一項所述之方法, 其中在方法步驟e)中進料該CO以使該反應在10巴至40巴之範圍的CO壓力下進行。
- 如申請專利範圍第1項至第5項中任一項所述之方法, 其中該方法包含額外的方法步驟g): g) 加入硫酸。
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MX2018015531A (es) | 2019-06-24 |
CN109942405B (zh) | 2021-09-17 |
CA3028186C (en) | 2021-01-12 |
ZA201808495B (en) | 2019-09-25 |
TWI798315B (zh) | 2023-04-11 |
KR102146328B1 (ko) | 2020-08-21 |
EP3502083B1 (de) | 2020-07-01 |
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