CN1018546B - 羧酸酯的还原方法 - Google Patents
羧酸酯的还原方法Info
- Publication number
- CN1018546B CN1018546B CN88102561A CN88102561A CN1018546B CN 1018546 B CN1018546 B CN 1018546B CN 88102561 A CN88102561 A CN 88102561A CN 88102561 A CN88102561 A CN 88102561A CN 1018546 B CN1018546 B CN 1018546B
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- disulfonic acid
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- 150000001733 carboxylic acid esters Chemical class 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 31
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims abstract description 22
- 239000000203 mixture Substances 0.000 claims abstract description 11
- 229910000033 sodium borohydride Inorganic materials 0.000 claims abstract description 11
- 239000012279 sodium borohydride Substances 0.000 claims abstract description 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 9
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 25
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- 229910052708 sodium Inorganic materials 0.000 claims description 3
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- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
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- 230000004913 activation Effects 0.000 description 2
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- YRHYCMZPEVDGFQ-UHFFFAOYSA-N methyl decanoate Chemical compound CCCCCCCCCC(=O)OC YRHYCMZPEVDGFQ-UHFFFAOYSA-N 0.000 description 2
- IJXHLVMUNBOGRR-UHFFFAOYSA-N methyl nonanoate Chemical compound CCCCCCCCC(=O)OC IJXHLVMUNBOGRR-UHFFFAOYSA-N 0.000 description 2
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- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 238000007086 side reaction Methods 0.000 description 2
- 239000001632 sodium acetate Substances 0.000 description 2
- 235000017281 sodium acetate Nutrition 0.000 description 2
- 229960004249 sodium acetate Drugs 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
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- ONGYZXKOUUTMRL-UHFFFAOYSA-N COC[O] Chemical compound COC[O] ONGYZXKOUUTMRL-UHFFFAOYSA-N 0.000 description 1
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
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- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
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- DPDMMXDBJGCCQC-UHFFFAOYSA-N [Na].[Cl] Chemical compound [Na].[Cl] DPDMMXDBJGCCQC-UHFFFAOYSA-N 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
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- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
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- UKVIEHSSVKSQBA-UHFFFAOYSA-N methane;palladium Chemical compound C.[Pd] UKVIEHSSVKSQBA-UHFFFAOYSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 210000004165 myocardium Anatomy 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- FBUKVWPVBMHYJY-UHFFFAOYSA-N noncarboxylic acid Natural products CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 1
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- 238000002360 preparation method Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/23—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing hydroxy or O-metal groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C50/00—Quinones
- C07C50/26—Quinones containing groups having oxygen atoms singly bound to carbon atoms
- C07C50/28—Quinones containing groups having oxygen atoms singly bound to carbon atoms with monocyclic quinoid structure
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/18—Preparation of ethers by reactions not forming ether-oxygen bonds
- C07C41/26—Preparation of ethers by reactions not forming ether-oxygen bonds by introduction of hydroxy or O-metal groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C46/00—Preparation of quinones
- C07C46/02—Preparation of quinones by oxidation giving rise to quinoid structures
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C46/00—Preparation of quinones
- C07C46/02—Preparation of quinones by oxidation giving rise to quinoid structures
- C07C46/04—Preparation of quinones by oxidation giving rise to quinoid structures of unsubstituted ring carbon atoms in six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C46/00—Preparation of quinones
- C07C46/02—Preparation of quinones by oxidation giving rise to quinoid structures
- C07C46/06—Preparation of quinones by oxidation giving rise to quinoid structures of at least one hydroxy group on a six-membered aromatic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
Abstract
Description
本发明涉及在合成药物时用作中间原料的10-(2-羟基-3,4-二甲氧基-6-甲基苯基)癸醇-1及其同类物的生产方法。
6-(10-羟癸基)-2,3-二甲氧基-5-甲基-1,4-苯醌(idebenone)已被公认是一种具有特殊药理活性的化合物,如其能增强免疫力,使肌肉松弛,对损伤组织,尤其是对心脏肌肉和脑组织,有使酶活化的作用,已知以工业方式生产idebenone的方法(Toku-Kai-Sho 59-39855)如下:
(第1步)-将9-(2-羟基-3,4-二甲氧基-6-甲基-苯甲酰基)壬酸烷基酯加以还原,产生10-(2-羟基-3,4-二甲氧基-6-甲基苯基)癸酸烷基酯。
(第2步)-产物用氢化双(2-甲氧乙氧基)铝钠(Vitride)作进一步还原,生成10-(2-羟基-3,4-二甲氧基-6-甲基苯基)癸醇-1。
(第3步)-将此新产物氧化,得到idebenone。
上述第2步中使用氢化双(2-甲氧乙氧基)铝钠有安全方面的问题,因为此化合物容易与空气中的水分发生作用放出氢而引燃。另外,此化合物又是一种特殊试剂,在稳定供应上也有困难。考虑到这些缺点,本发明者于是进行了各方面的研究,发现采用硼氢化钠与氯化铝的混合物作为还原剂,应用于生产10-(2-羟基-3,4-二甲氧基-6-甲基苯基)癸醇-1及其同类物时,可得到令人满意的产率,并可工业规模生产。
本发明是有关下式化合物的生产方法:
式中R1和R2各代表一个低级烷基;n表示0至21的整数,X代表氢原子或一任意被保护的羟基;Y代表一任意被保护的羟基,该方法包括如何用硼氢化钠与氯化铝混合物还原下式所示酯类化合物:
式中R1、R2、n、X和Y代表与上述相同的含义,R3代表低级烷基。
上述(Ⅰ)式和(Ⅱ)式中R1、R2和R3所代表的低级烷基的实例包括碳原子数1至4的烷基,诸如甲基、乙基、丙基等基团;X和Y代表的任意被保护的羟基除自由羟基外,例如有碳原子数1至3的低级烷氧基(甲氧基,乙氧基等),碳原子数为2至4的低级酰氧基(乙酰氧基、丙酰氧基等),碳原子数从3至6的硅烷氧基(三甲基硅烷氧基等),甲氧基甲基氧等,n代表0至21的整数,以8至12最佳。
本发明的还原反应最好在适当的溶剂中进行。任何能溶解起始化合物(Ⅰ)而不阻碍反应进行的溶剂均可选用。此类溶剂的实例包括醚类如乙醚,四氢呋喃、二氧杂环己烷等,以及苯、甲苯、二甲苯等芳
烃类。反应温度一般在0°至140℃之间,以10°至40℃为最佳。硼氢化钠用量一般不少于起始化合物(Ⅰ)摩尔数的1.5倍,取其摩尔数的2倍量左右为好。氯化铝的用量最好是使其与硼氢化钠的摩尔比约为1∶3。
若体系中有少量水存在,反应的结果更好。更具体地说,水的存在抑制了不期望的副反应产物(即式(Ⅱ)化合物,其中R1和R2中之一是氢或两者均是氢)的生成,因而期望的化合物(Ⅱ)的产率便得到进一步的改善。所加入的水量一般在0.1至1.7倍摩尔数的范围内,最好是0.2至1.5倍。加入过量水,期望的化合物不能获得高产量,而且反应时间拖长。
本发明所得的化合物(Ⅱ)可以用能将酚转化成醌而不影响醇羟基的氧化剂进行氧化,可导至下式化合物的生成
式中符号所代表的意义同上。这些氧化剂可以是氧化银、氯化高铁、二氧化锰、亚硝基二磺酸盐等,其中以亚硝基二磺酸的二碱金属盐为最可取,这化合物可通过电解羟胺二磺酸二碱金属的水溶液,使之进行氧化反应的方法得到。
下面是采用通过电解氧化羟胺二磺酸二碱金属盐水溶液而得到的亚硝基二磺酸二碱金属盐作为氧化剂对化合物(Ⅱ)进行氧化反应的说明。
羟胺二磺酸二碱金属盐可以二钠盐或二钾盐为例,而亚硝基二磺酸二碱金属盐也可以二钠盐或二钾盐为例,以选用亚硝基二磺酸二钠盐更佳。
进行化合物(Ⅱ)的氧化是先将该化合物溶于诸如甲醇、乙醇、二氧杂环己烷、四氢呋喃等与水互溶的溶剂中,然后加入亚硝基二磺酸二碱金属盐。其加入量如按其与化合物(Ⅱ)的化学计量计算,应为其摩尔数的2.0倍,但考虑到亚硝基二磺酸二碱金属盐的稳定性,通常加入量为其摩尔数的2.6倍或更多,最好3.0倍或更多,反应温度在20°至70℃之间,以50℃左右最好。温度太低,反应速度太慢;反应温度太高亚硝基二磺酸二碱金属盐的分解加快,不希望有的副反应也容易发生,这是我们所不希望的。反应时间随起始化合物(Ⅰ)的浓度、所用的溶剂种类、亚硝基二磺酸二碱金属盐的用量以及反应温度等条件而变化,但通常一旦起始化合物消耗完毕,反应即停止。举例来说,用薄层色谱、高效液相色谱、气相色谱等方法跟踪,起始物料随时间减少,发现当起始物料不再被检出时,反应即终止。反应在50℃进行时,通常在两小时内即可完全。作为氧化剂的亚硝基二磺酸二碱金属盐的水溶液可通过电解羟胺二磺酸二碱金属盐的水溶液使之氧化而获得,电解可在一般化学电池中进行,化学电池可装有隔板或隔膜,通常以采用压力过滤器型装有阳离子交换膜的电化学电池最为可取,反应所放出的热可通过缩小电极间隙控制电池电压的升高、以及在电池外冷却高速循环于两电池室的阳极液和阴极液等方法来加以抑制。阳极和阴极可用任何通用于电化学领域的电极材料,如碳、铂、不锈钢、钯、镍、镍合金等。一般最乐于采用不锈钢网状电极。电解池可配上一搅拌装置,也可用泵加速反应液的循环。
进行电解氧化反应时可将羟胺二磺酸二碱金属盐的水溶液加以0.5至50伏的电压,以2至20伏为最适宜。通过溶液的电流密度可达每平方分米50安培。最好取用2至20安培。为使电解氧化反应的进行更有效,可在水溶液中加入常用的电解质,如氢氧化钠、醋酸钠、碳酸钠、碳酸氢钠、磷酸钠、氯化钠等。电解质的加入量一般相当于水溶液重量的0.1至30%。欲进行电解氧化反应的水溶液所含羟胺二磺酸二碱金属盐的浓度一般每升溶液至少含0.1摩尔,最佳范围是0.1至2摩尔。电解氧化反应的温度在-15°至50℃之间。一般以0°至35℃的范围最佳。反应时间至少0.5小时或更长,一般情况下反应应进行1至10小时。
电解氧化反应开始时,羟胺二磺酸二碱金属盐的水溶液pH值调在10与13之间,最好调在11.5左右,这样可使亚硝基二磺酸二碱金属盐的产量最高。
化合物(Ⅲ)能增强免疫力,有松弛肌肉的作用,还有能促使脑组织中酶的活化作用等。
本发明所用的起始化合物(Ⅰ)可以用一般的还原方法将以下述通式表示的化合物还原而得到:
式中符号所代表的意义同上。一般的还原方法有如利用锌汞齐和盐酸的Clemensen还原法、Wolff-Kishner腙还原法,二硫缩醛的
脱硫还原法,或催化还原法。
本发明利用硼氢化钠和氯化铝的混合物将化合物(Ⅰ)还原,得到高产量的化合物(Ⅱ)。若于反应体系中加入水,欲得的化合物(Ⅱ)不但产量高、纯度高,且重现性也好。
本发明将以下列实例和参考例作更进一步的详细说明。
参考例1
于9-(2-羟基-3,4-二甲氧基-6-甲基苯甲酰基)壬酸甲酯(2.0千克)的乙酸乙酯(10升)溶液中加入5%的钯碳黑(含水50%)(400克)和硫酸(10毫升)。混合物在30°至40℃通入氢气流(氢气压力约8.5千克/厘米2G)的条件下搅拌5小时。滤去催化剂,将乙酸乙酯层用水(10升)、用5%碳酸氢钠(10升)、再用水(10升)逐次洗涤。乙酸乙酯层经过浓缩后便可获得油状的10-(2-羟基-3,4-二甲氧基-6-甲基苯基)癸酸酯(1.8千克)产品。红外吸收光谱的λ薄膜 最大厘米-1为:3450(OH),1740(COOCH2)。核磁共振谱δ
为:1.10至1.87(14H,多重谱线,-(CH2)7-),2.17至2.57(4H,多重谱线,环CH2,CH2CO)、2.27(3H、单谱线,环CH2),3.63(3H,单谱线,COOCH3),3.80(3H,单谱线,OCH2),3.85(3H,单谱线,OCH3),5.80(1H,单谱线,OH),6.27(1H,单谱线,环H)
实例1
溶解10-(2-羟基-3,4-二甲氧基-6-甲基苯基)癸酸甲酯(881克,2.5摩尔)于1.8升四氢呋喃中。再在此溶液中加入硼氢化钠(340克、9摩尔)的四氢呋喃(10.7升)悬浮液,然后将此混合物搅拌。于所得的混合物悬浮液中加入水(75毫升,4.16摩尔),
另将氯化铝(400克,3摩尔)溶解于四氢呋喃(6.0升)中。在90分钟内,以给定的速度将此溶液逐滴加到上述悬浮液中,在此期间反应物的内部温度应保持在25±2℃。然后,在相同的温度条件下再将反应物继续搅拌30分钟,并将之冷却至约15℃,往里逐滴加入水(22升),使发生分解反应,然后再逐滴加入盐酸(2.7升)。混合物用甲苯萃取两次,每次9升。合併两份甲苯层,先用碳酸氢钠(4.4升)的5%水溶液洗,再用水(4.4升)进一步洗涤,将甲苯层减压浓缩,便可得到10-(2-羟基-3,4-二甲氧基-6-甲基苯基)癸醇-1(805克,2.48摩尔,产率99.2%)的油状产品。红外吸收光谱ν净 最大cm-1为:3400(OH)左右。核磁共振谱为δ
:1.10至1.80(16H,多重谱线,-(CH2)8-,2.22(3H,单谱线,CH2),2.40至2.75(2H,多重谱线,CH2),8.50至8.70(2H,多重谱线,CH2),3.80(3H,单谱线,OCH2),8.84(3H,单谱线,OCH2),6.25(1H,单谱线,环H)。
实例2
对水的加入量与10-(2-羟基-3,4-二甲氧基-6-甲基苯基)癸醇-1的产量之间的关系进行了研究。将10-(2-羟基-3,4-二甲氧基-6-甲基苯基)癸羧甲酯(17.3克,49.1毫摩尔)溶于四氢呋喃(35.7毫升)中,加到硼氢化钠(6.8克,80毫摩尔)的四氢呋喃(214.5毫升)悬浮液中,搅拌此混合物。将准确量过(如表1所述)体积的水加到此悬浮液中。用四氢呋喃(142毫升)溶解氯化铝(8.0克,60毫摩尔)。将此溶液在内部温度为25±2℃条件下,在90至120分钟内逐滴加至上述悬浮液中。继续保持温度25±2℃,将反应物搅拌30分钟。然后将反应物冷却至15±2℃,并逐滴加入水(446毫升)。
再缓慢地逐滴加入盐酸(53.5毫升),在此期间反应物的温度要求不超过20℃。接着反应物用甲苯萃取两次,每次178.5毫升。合併两份甲苯层,用水(89.5毫升)洗涤两次。把甲苯层减压浓缩,便可获得10-(2-羟基-3,4-二甲氧基-6-甲基苯基)癸醇-1的油状产物。表1示出所加入的水的体积与癸醇化合物的产率及所产生的二羟基化合物的量之间的关系。
表1 加入的水的体积与癸醇化合物的产率及所产生的二羟基化合物的量之间的关系
编号 加入的水的体积 癸醇化合物的产率 二羟基化合物
毫升数 摩尔比1) (%) 的产率2)(%)
1 0 0.0 94.2 9.2
2 0 0.0 95.4 6.9
3 0.8 0.74 96.9 3.3
4 0.8 0.74 98.2 2.8
5 1.0 0.93 98.3 1.8
6 1.0 0.93 98.3 2.7
7 1.5 1.39 99.2 0.6
8 1.5 1.39 99.2 1.4
9 1.8 1.67 99.0 1.2
10 1.8 1.67 98.7 1.7
11 2.0 1.85 97.6 0.5
12 2.0 1.85 90.4 0.0
13 2.5 2.31 85.3 0.0
14 2.5 2.31 90.6 0.0
注1)
摩尔比= (加入的水的摩尔数)/(氯化铝摩尔数)
注2)
二羟基化合物的产率= (二羟化合物的峰面积)/(癸醇化合物的峰面积) ×100
二羟基化合物:10-(2,3-二羟基-4-甲氧基-6-甲基苯基)癸醇-1
参考例2
羟胺二磺酸二钠盐水溶液的合成
溶解亚硝酸钠(1875克)于水(7.5升)中,然后逐滴加入35%重量的亚硫酸氢钠水溶液(11.5升),同时保持溶液温度为0℃或更低。混合溶液中再逐滴加入醋酸(2,860毫升),同时使温度不超过5℃,在此温度条件下继续搅拌溶液90分钟。然后在10℃或更低温度下再逐滴加入30%重量的苛性钠水溶液(3,125毫升),再逐滴加入25%重量的碳酸钠水溶液(20升),便可获得能直接进行电解氧化的羟胺二磺酸二钠盐的水溶液。产量约为84%。
参考例3
用电解氧化反应合成亚硝基二磺酸二钠盐的水溶液。
单极、双室型和压力过滤器型的电化学电池(有效电极面积:4.5分米2/电池×2电池)中放入羟胺二磺酸二钠盐水溶液(6至8升)作为阳极液。碳酸钠的10%重量水溶液(6至8升)作为阴极液,再用泵使溶液进行循环。在给定的电解条件下(电流密度:8安/分米2,循环线性速度:10.4厘米/秒,温度:15℃)通电2至3小时,得
到亚硝基二磺酸二钠的水溶液,产率为或大于90%。
参考例4-7
溶解10-(2-羟基-3,4-二甲氧基-6-甲基苯基)癸醇-1(271克)于甲醇(5.4升)中,于其中加入用电解氧化反应合成的亚硝基二磺酸二钠的水溶液(6.7升,浓度为0.359摩尔/升),保持温度在50±2℃,搅拌此混合溶液2小时。用薄层色谱法证实起始物料已告消失后,反应混合物中加入水(8.6升),继用甲苯萃取二次(5.5升及2.7升)。合併二次甲苯萃取液,用水洗涤。进行减压浓缩:得6-(10-羟基癸基)-2,3-二甲氧基-5-甲基-1,4-苯醌粗品(288克,含量94.8%、产率96.9%)。粗品(20克)从甲苯(60毫升)与正己烷(180毫升)混合溶剂中重结晶。结晶用甲苯(60毫升)溶解,并使此溶液通过活性氧化铝(30克)涂层。减压浓缩此流出液,浓缩液再从甲苯(55毫升)与正己烷(165毫升)的混合液中重结晶一次。又从50%乙醇(108毫升)中进一步重结晶。干燥后得到16.2克橙黄色的6-(10-羟基癸基)-2,3-二甲氧基-5-甲基-1,4-苯醌结晶,熔点54.0℃。
红外吸收光谱νKBr 最大厘米-1:3550(OH),1660,1650,1610(1,4-苯醌)
核磁共振谱δ
:1.1至1.8(16H,多重谱线,-(CH2)8-)92.00(3H,单谱线,CH2),2.43(2H,三重谱线,J=7Hz,CH2),3.63(2H,三重谱线,J=6Hz,CH2OH),3.97(6H,单谱线,OCH3)
用通过电解氧化反应合成的亚硝基二磺酸二钠水溶液的各种实例均列述于表2
表2 用通过电解氧化反应制备的亚硝基二磺酸二钠水溶液进行1的
氧化
实例编号 加入量 反应条件2 ~
1 ~ 3 ~CH3OH 温度 时间 产量 产率
(克) (摩尔/升) (升) (℃) (小时) (克) (%)
4 271 2.41/6.7 5.4 48-53 2.0 273 96.9
5 262 2.32/6.7 5.2 48-53 2.0 266 97.3
6 308 2.96/7.6 6.1 48-52 2.0 318 98.9
7 372 3.40/7.6 7.6 48-50 2.0 380 98.0
参考例8-10
将10-(2-羟基-3,4-二甲氧基-6-甲基苯基)癸醇-1(6.84千克)溶于甲醇(110升)中,于其中加入醋酸钠(27.4千克)与水(110升)。往此混合物中加入亚硝基二磺酸二钾盐(23.5千克,含量69.9%),混合液在温度50±3℃下搅拌3小时。用薄层色谱法检
查证实起始物料消失后,加入水(550升),在或低于10℃下搅拌30分钟或更长,离心分离析出的结晶。收集结晶,溶于乙酸乙酯(40升)中,用水(25升)洗涤。减压浓缩乙酸乙酯层,得到6-(10-羟基癸基)-2,3-二甲氧基-5-甲基-1,4-苯醌粗品(6.70千克,产率93.9%)。采用亚硝基二磺酸二钾盐(Fremy盐)的实例均列于表3。
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JPS5919930B2 (ja) * | 1974-05-02 | 1984-05-09 | 武田薬品工業株式会社 | キノン酸誘導体の製造法 |
JPS567734A (en) * | 1979-06-28 | 1981-01-27 | Takeda Chem Ind Ltd | Preparation of quinone derivative |
JPS56147746A (en) * | 1980-04-15 | 1981-11-16 | Takeda Chem Ind Ltd | Quinones and their preparation |
FI75561C (fi) * | 1979-10-30 | 1988-07-11 | Ciba Geigy Ag | Foerfarande foer framstaellning av 5- karbamoyl-10-oxo-10,11-dihydro-5h-dibens/b,f/azepin och daertill noedvaendiga mellanprodukter. |
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1988
- 1988-04-21 AT AT88303622T patent/ATE80141T1/de not_active IP Right Cessation
- 1988-04-21 ES ES88303622T patent/ES2051841T3/es not_active Expired - Lifetime
- 1988-04-21 EP EP88303622A patent/EP0289223B1/en not_active Expired - Lifetime
- 1988-04-21 DE DE8888303622T patent/DE3874195T2/de not_active Expired - Fee Related
- 1988-04-22 DK DK219288A patent/DK219288A/da not_active Application Discontinuation
- 1988-04-25 KR KR1019880004727A patent/KR960002597B1/ko not_active IP Right Cessation
- 1988-04-26 WO PCT/JP1988/000406 patent/WO1988008415A1/en unknown
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- 1988-04-26 HU HU882100A patent/HU199378B/hu not_active IP Right Cessation
- 1988-04-26 PL PL1988282657A patent/PL158961B1/pl unknown
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- 1988-04-26 CA CA000565050A patent/CA1290760C/en not_active Expired - Lifetime
- 1988-04-26 US US07/186,297 patent/US4842775A/en not_active Expired - Lifetime
- 1988-04-27 NZ NZ224402A patent/NZ224402A/xx unknown
- 1988-04-27 JP JP63106200A patent/JPH0832655B2/ja not_active Expired - Fee Related
- 1988-04-27 CN CN88102561A patent/CN1018546B/zh not_active Expired
- 1988-09-19 SU SU4356640A patent/SU1768029A3/ru active
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1992
- 1992-04-07 CN CN92102604A patent/CN1033855C/zh not_active Expired - Fee Related
- 1992-10-22 GR GR920402385T patent/GR3006060T3/el unknown
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1995
- 1995-08-17 DK DK092295A patent/DK92295A/da not_active Application Discontinuation
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