噻吩类化合物是仅含有一个硫原子的五元杂环化合物,基本骨架为噻吩。这种化合物主要存在于煤焦油和页岩油中。
相较于苯,噻吩更为活泼。它具有光敏性,在光照条件下会发生碳架重排;可以与金属反应;在阮内镍的作用下可脱除硫原子;还能够进行取代反应(多发生在2位);可以氧化开环,并生成不同产物;可以在2、5位发生硝化,形成硝基噻吩;卤化后可产生2位单卤化物、2,5-位二卤化物、2,3,5-三卤化物及四卤化物;与苯缩合能生成苯并噻吩。
由于硫的非共用电子对与两个碳原子结合,噻吩环形成了一个6π电子系统,并表现出芳香族性质。因此它可以进行硝化、磺化和卤化等亲电取代反应,取代位置通常为2-位和5-位。这类反应比苯更容易发生。例如,在温和的缩合剂如正磷酸存在下,噻吩即可发生Friedel-Crafts反应,在α-位引入酰基。
在硝酸作用下,与碘反应可以高产率制备2-碘噻吩;Mannich反应也可用于合成2-噻吩甲胺。
噻吩广泛应用于生产染料、香料、耐急冷急热塑料、高活性溶剂、刺激素、杀虫剂、增亮剂、化妆品以及生物活化物质和维生素、麻醉剂及抗菌素等药物。尽管可以通过化学方法制备,但由于成本较高,实际应用中噻吩主要从粗苯的预精馏轻苯中提取。
在轻苯酸洗精制过程中,噻吩会与硫酸反应生成噻吩磺酸,并溶解于废硫酸中;通过澄清、除去焦油状物质及水解蒸馏处理后,可得到含噻吩和苯族烃的粗馏油。进一步碱中和至中性或微碱性后,使用理论板数为30~40的精馏塔进行精馏,可以分离出高纯度的噻吩产品。而剩余残液则可用于精馏出间-二甲苯约95%含量的产品。
中文名称 | 英文名称 | CAS号 | 化学式 | 结构式图片 |
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2-苯甲酰噻吩 | 2-Benzoylthiophene | 135-00-2 | C11H8OS |
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2-苯基噻吩 | 2-phenylthiophene | 825-55-8 | C10H8S |
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2-苄基噻吩 | 2-benzylthiophene | 13132-15-5 | C11H10S |
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2-羟基-5-溴噻吩 | 5-bromothiophen-2-ol | 1313392-39-0 | C4H3BrOS |
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2-羟基-2,2-双(2-噻吩)乙酸 | 2-hydroxy-2,2-di(thiophen-2-yl)acetic acid | 4746-63-8 | C10H8O3S2 |
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2-羟基-1,2-二(2-噻吩基)乙烷-1-酮 | thenoin | 27761-02-0 | C10H8O2S2 |
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2-碘噻吩 | 2-Iodothiophene | 3437-95-4 | C4H3IS |
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2-碘-苯并[b]噻吩 | 2-iodobenzothiophene | 36748-89-7 | C8H5IS |
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2-碘-5-甲基噻吩 | 2-iodo-5-methylthiophene | 16494-36-3 | C5H5IS |
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2-硫苯基噻吩 | 2-(Phenylthio)thiophene | 16718-12-0 | C10H8S2 |
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2-硝基噻吩-4-腈 | 4-nitrothiophene-2-carbonitrile | 42137-24-6 | C5H2N2O2S |
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2-硝基噻吩-4-甲醛 | 5-nitrothiophene-3-carboxaldehyde | 75428-45-4 | C5H3NO3S |
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2-硝基噻吩 | 2-nitrothiophene | 609-40-5 | C4H3NO2S |
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2-硝基乙烯基噻吩 | 2-(2-nitroethenyl)thiophene | 874-84-0 | C6H5NO2S |
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2-甲醇-4-甲基噻吩 | (4-methylthiophen-2-yl)methanol | 74395-18-9 | C6H8OS |
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2-甲酰胺-5-(2-巯基-1,3-噻唑-4-基)-噻吩 | 5-(2-mercapto-4-thiazolyl)thiophene-2-carboxamide | 52560-89-1 | C8H6N2OS3 |
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2-甲酰基噻吩-3-羧酸 | 2-formylthiophene-3-carboxylic acid | 19991-69-6 | C6H4O3S |
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2-甲氧基噻吩 | 2-methoxythiophene | 16839-97-7 | C5H6OS |
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2-甲巯基吩噻嗪 | 2-(methylthio)-10H-phenothiazine | 7643-08-5 | C13H11NS2 |
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2-甲基苯并噻吩 | 2-Methylbenzothiophene | 1195-14-8 | C9H8S |
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2-甲基苯并[b]噻吩-3-羧醛 | 2-methylbenzo[b]thiophene-3-carbaldehyde | 30446-99-2 | C10H8OS |
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2-甲基磺酰噻吩 | 2-(methylsulfonyl)thiophene | 38695-60-2 | C5H6O2S2 |
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2-甲基四氢噻吩 | 2-methylthiolane | 1795-09-1 | C5H10S |
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2-甲基噻吩并噻唑 | methyl-2 thieno<2,3-d>thiazole | 61612-02-0 | C6H5NS2 |
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2-甲基-5-苯基噻吩 | 2-methyl-5-phenylthiophene | 5069-26-1 | C11H10S |
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2-甲基-4H-噻吩并[3,2-b]吡咯-5-羧酸 | 2-methyl-4H-thieno[3,2-b]pyrrole-5-carboxylic acid | 332099-14-6 | C8H7NO2S |
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2-甲基-3-噻吩甲酸甲酯 | methyl 2-methylthiophene-3-carboxylate | 53562-51-9 | C7H8O2S |
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2-甲基-3-噻吩甲酸乙酯 | ethyl 2-methyl-thiophene-3-carboxylate | 19432-66-7 | C8H10O2S |
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2-甲基-3-噻吩甲酸 | 2-methylthiophene-3-carboxylic acid | 1918-78-1 | C6H6O2S |
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2-溴苯并噻吩 | 2-bromo-1-benzothiophene | 5394-13-8 | C8H5BrS |
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2-溴甲基噻吩 | 2-thenyl bromide | 45438-73-1 | C5H5BrS |
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2-溴噻吩并[3,2-b]噻吩 | 2-bromothieno[3,2-b]thiophene | 25121-82-8 | C6H3BrS2 |
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2-溴噻吩-5-甲醇 | (5-bromothien-2-yl)methanol | 79387-71-6 | C5H5BrOS |
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2-溴噻吩-4-甲醛 | 5-bromo-3-thiophenecarbaldehyde | 18791-79-2 | C5H3BrOS |
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2-溴噻吩-3-腈 | 2-bromo-3-cyanothiophene | 56182-43-5 | C5H2BrNS |
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2-溴噻吩-3-胺 | 2-bromothiophen-3-amine | 106944-13-2 | C4H4BrNS |
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2-溴噻吩-3-甲醛 | 2-bromothiophene-3-carbaldehyde | 1860-99-7 | C5H3BrOS |
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2-溴噻吩 | 2-bromothiophene | 1003-09-4 | C4H3BrS |
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2-溴二苯并噻吩 | 2-bromodibenzothiophene | 22439-61-8 | C12H7BrS |
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2-溴-5-苯甲酰基噻吩 | 2-benzoyl-5-bromothiophene | 31161-46-3 | C11H7BrOS |
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2-溴-5-碘噻吩 | 5-iodo-2-bromothiophene | 29504-81-2 | C4H2BrIS |
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2-溴-5-碘-3-己基噻吩 | 2-bromo-5-iodo-3-hexylthiophene | 160096-76-4 | C10H14BrIS |
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2-溴-5-硝基噻吩 | 2-bromo-5-nitrothiophene | 13195-50-1 | C4H2BrNO2S |
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2-溴-5-甲基噻吩 | 2-bromo-5-methyl thiophene | 765-58-2 | C5H5BrS |
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2-溴-5-氯噻吩 | 5-bromo-2-chlorothiophene | 2873-18-9 | C4H2BrClS |
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2-溴-5-氯-3-甲基苯并[B]噻酚 | 2-bromo-5-chloro-3-methylbenzo[b]-thiophene | 175203-60-8 | C9H6BrClS |
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2-溴-5-正丙基噻吩 | 2-bromo-5-propylthiophene | 172319-75-4 | C7H9BrS |
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2-溴-5-乙基噻吩 | 2-bromo-5-ethylthiophene | 62323-44-8 | C6H7BrS |
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2-溴-5-丁基噻吩 | 2-bromo-5-butylthiophene | 128619-83-0 | C8H11BrS |
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2-溴-5-(三氟甲基)噻吩 | 2-bromo-5-(trifluoromethyl)thiophene | 143469-22-1 | C5H2BrF3S |
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