酰卤
酰卤是一类含有卤素原子(如氯、溴等)和羰基官能团的化合物,通式为R-CO-X,其中R代表一个烷基、芳基或其他烃基团,X表示卤素。这类化合物因其在有机合成中具有重要应用而受到广泛关注。
1. 物理性质 酰卤通常为无色液体或固体,在常温下较为稳定,但在较高温度时会发生水解反应生成相应的羧酸和卤化氢。例如,乙酰氯(CH3COCl)是无色易挥发的油状液体,而乙酸酐(CH3CO)2O则为有刺激性气味的无色透明液体。
2. 化学性质
水解反应:酰卤能够与水迅速反应生成相应的羧酸和卤化氢气体。例如: [ R-CO-X + H_2O → R-COOH + HX ]
亲核取代反应:这类化合物也是良好的离去基团,可以用于亲核取代反应,如傅-克酰基化反应等。 [ R'-OH + R-COCl → R'-COR + HCl ]
3. 应用 酰卤因其较高的活性和选择性,在有机合成中具有重要应用价值。它们常被用来作为中间体来引入羰基,进而用于合成各种重要的药物、农药、香料等化合物。
药物合成:由于其高反应性和稳定性,酰卤常用于制备特定结构的药物分子。
合成其他化学品:通过与多种亲核试剂发生反应,可以合成酯、酸酐等多种衍生物。
总的来说,酰卤是一类多功能且广泛应用的有机化合物,在有机化学领域占据着重要位置。
中文名称 | 英文名称 | CAS号 | 化学式 | 结构式图片 |
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—— | 3,6-Dithiaoctandioyl-dichlorid | 31249-80-6 | C6H8Cl2O2S2 |
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—— | 3-chloro-4-methoxybutyryl chloride | 1072151-75-7 | C5H8Cl2O2 |
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—— | (E)-4-methoxybut-2-enoyl chloride | 1072420-11-1 | C5H7ClO2 |
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—— | 2-(1-Adamantyl)-3,3-dimethylbutanoyl chloride | 125312-59-6 | C16H25ClO |
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—— | palmitoyl iodide | 127421-45-8 | C16H31IO |
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—— | bromoacetic-2,2-d2 acid bromoanhydride | 40897-88-9 | C2H2Br2O |
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—— | 3-Ethoxy-2,2-dimethylpropanoyl chloride | 87637-07-8 | C7H13ClO2 |
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—— | 5-bromo-4,4-dimethylvaleryl chloride | 140629-09-0 | C7H12BrClO |
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—— | 5-bromo-2,2-dimethylpentanoic chloride | 140629-08-9 | C7H12BrClO |
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—— | 5-bromo-2-methylpentanoyl chloride | 140629-11-4 | C6H10BrClO |
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—— | O-propyl-lactic acid-chloride | 120675-25-4 | C6H11ClO2 |
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—— | (+/-)-<i>trans</i>-methyl-cyclohexanecarbonyl chloride | 13064-91-0 | C8H13ClO |
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—— | 3-Chlor-cyclobutan-dicarbonsaeure-(1,1)-dichlorid | 89582-02-5 | C6H5Cl3O2 |
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—— | 3-chlorocyclobutane carboxylic acid chloride | 30494-32-7 | C5H6Cl2O |
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—— | 2-bromo-hexadecanoyl bromide | 95605-11-1 | C16H30Br2O |
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—— | 2-n-pentylheptanoyl chloride | 100246-66-0 | C12H23ClO |
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—— | ω-chloroperfluoropelargonyl chloride | 2925-59-9 | C9Cl2F16O |
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—— | 2-hexyloctanoic acid chloride | 77582-73-1 | C14H27ClO |
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—— | 4-pentenoyl fluoride | 719301-32-3 | C5H7FO |
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—— | 4,4-dimethyl<2,2-2H2>pentanoyl chloride | 153187-06-5 | C7H13ClO |
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—— | 4,4-dimethyl<3,3-2H2>pentanoyl chloride | 153187-05-4 | C7H13ClO |
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—— | 2-Brom-3,3-dimethylbutyrylbromid | 74702-95-7 | C6H10Br2O |
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—— | cycloheptyl-acetyl chloride | 84676-49-3 | C9H15ClO |
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—— | 2-methyltetradecanoyl chloride | 77748-01-7 | C15H29ClO |
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—— | 5-ethoxy-valeryl chloride | 121481-63-8 | C7H13ClO2 |
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—— | 2-cyano-2-methylpropanoyl chloride | 50648-67-4 | C5H6ClNO |
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—— | (E)-2-(trimethylsilylmethyl)hept-2-enoyl chloride | 405297-75-8 | C11H21ClOSi |
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—— | diisobutyl-malonyl chloride | 160191-78-6 | C11H18Cl2O2 |
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—— | 2,3-dichloro-succinyl chloride | 54732-67-1 | C4H2Cl4O2 |
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—— | maleic acid dichloroanhydride | 22542-53-6 | C4H2Cl2O2 |
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—— | fumaroyl bromide | 117921-67-2 | C4H2Br2O2 |
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—— | Butylethylmalonylchlorid | 5659-94-9 | C9H14Cl2O2 |
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—— | α-Iod-isobuttersaeurechlorid | 54468-35-8 | C4H6ClIO |
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—— | fluorure d'acide suberique | 13022-56-5 | C8H12F2O2 |
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—— | 4-iodobutanoyl chloride | 927-59-3 | C4H6ClIO |
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—— | 1,5-Pentandicarbonsaeuredifluorid | 13082-35-4 | C7H10F2O2 |
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—— | (1<i>S</i>)-1,2,2,3<i>c</i>-tetramethyl-cyclopentane-<i>r</i>-carbonyl chloride | 59642-06-7 | C10H17ClO |
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—— | 1,2,2,3-tetramethyl-cyclopentanecarbonyl chloride | 119008-74-1 | C10H17ClO |
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—— | 2-bromodecanoyl chloride | 99217-33-1 | C10H18BrClO |
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—— | 3,4-dimethylpentanoic acid chloride | 137586-00-6 | C7H13ClO |
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—— | (E)-4-bromo-4-methylpent-2-enoyl chloride | 144139-18-4 | C6H8BrClO |
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—— | 2-bromo-3-cyclohexylpropanoyl chloride | 557799-48-1 | C9H14BrClO |
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—— | (1R,3S)-camphoric acid dichloride | —— | C10H14Cl2O2 |
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—— | 2-methyl-4-pentenoyl chloride | 149065-49-6 | C6H9ClO |
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—— | Muconsaeure-dichlorid | 20578-72-7 | C6H4Cl2O2 |
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—— | bromo-cyclopropyl-acetyl chloride | 1010802-72-8 | C5H6BrClO |
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—— | 2,4,4-trimethyl-valeryl chloride | 5340-42-1 | C8H15ClO |
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—— | 2-bromomethylpropionyl bromide | 56970-80-0 | C4H6Br2O |
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—— | 2-Ethyl-hexan-carbonsaeure-1-chlorid | 114182-65-9 | C9H17ClO |
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—— | hexyloxy-acetyl chloride | 63579-01-1 | C8H15ClO2 |
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