二环己基甲酮
外观
(重定向自119-60-8)
二环己基甲酮 | |
---|---|
英文名 | Dicyclohexylmethanone Dicyclohexyl ketone |
识别 | |
CAS号 | 119-60-8 |
EINECS | 204-336-0 |
性质 | |
化学式 | C13H22O |
摩尔质量 | 194.31 g·mol⁻¹ |
密度 | 0.986 g/mL[1] |
熔点 | 61 °C[2] |
沸点 | 138 °C (13 mmHg)[1] 159 °C (20 Torr)[3] |
折光度n D |
1.486 (589.3 nm, 20 °C)[4] |
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。 |
二环己基甲酮是一种有机化合物,化学式为C13H22O,该化合物可看作丙酮的甲基替换为环己基。二环己基甲酮可燃,其燃烧产物为碳氧化物。[5]
合成
[编辑]二环己基甲酮可以由环己酰氯和环己基溴化镁反应得到。[6]环己腈和格氏试剂的反应也能得到二环己基甲酮。[7]
性质
[编辑]二环己基甲酮的羰基可以和三乙基硅烷在二氯甲烷中反应,在一种苯并喹啉茂基铱催化剂的存在下,生成(C6H11)2CH-O-Si(C2H5)3。[8]它也可以和苯肼盐酸盐在乙酸中回流,制得含氮杂环化合物:[9]
它在铁催化剂(如乙酰丙酮铁)的存在下可以被三乙基硼氢化钠还原为相应的醇。[10]以锂粉-萘-无水氯化镍作为还原体系,在四氢呋喃溶剂中对其进行还原,在室温下便可得到相应的醇。[11]
甲基溴化镁与其作用得到的是1,1-二环己基乙醇。[12]
二环己基甲酮在5~10 °C和三溴化磷进行溴化反应,得到二溴代产物二(1-溴环己基)甲酮。[13]
参考文献
[编辑]- ^ 1.0 1.1 二环己基甲酮 (119-60-8) CAS数据库. Chemical Book. [2018-7-16]
- ^ Venus-Danilova, E. D.; Transformation of asymmetric dicyclohexylethylene oxide J. Russ. Phys.-Chem. Soc. 1929, 61, pp 1479-1484 CAPLUS
- ^ Mousseron, Max; Granger, Robert. Alicyclic series. VI. The organomagnesium compounds. Bulletin de la Societe Chimique de France 1946, pp 251-256 CAPLUS
- ^ Smushkevich, Yu. I.; Belov, V. N.; Kleev, B. V.; Golger, A. Ya. Reaction of aldehydes with olefins. I. Reaction of aldehydes with cyclohexene. Zhurnal Obshchei Khimii. 1964, V34(11), P3815-17 CAPLUS
- ^ 二环己基甲酮 化学品安全技术说明书. SigmaAldrich. [2018-7-16]
- ^ Mousseron, Max; Granger, Robert. Alicyclic series. VI. The organomagnesium compounds. Bulletin de la Societe Chimique de France. 1946. 251-256.
- ^ Canonne, Persephone; Foscolos, George B.; Lemay, Gilles. Effet du benzene dans la reaction de Grignard sur les nitriles(法文). Tetrahedron Letters, 1980. 21 (2): 155-158. doi:10.1016/S0040-4039(00)71400-6
- ^ Hamdaoui, Mustapha; Desrousseaux, Camille; Habbita, Houda; Djukic, Jean-Pierre. Iridacycles as Catalysts for the Autotandem Conversion of Nitriles into Amines by Hydrosilylation: Experimental Investigation and Scope. Organometallics, 2017. 36 (24): 4864-4882. doi:10.1021/acs.organomet.7b00749
- ^ Bakulina, Olga; Ivanov, Alexander; Suslonov, Vitalii; Dar'in, Dmitry; Krasavin, Mikhail. A speedy route to sterically encumbered, benzene-fused derivatives of privileged, naturally occurring hexahydropyrrolo[1,2-b]isoquinoline. Beilstein Journal of Organic Chemistry, 2017 (13): 1413-1424. doi:10.3762/bjoc.13.138
- ^ Tamang, Sem Raj; Findlater, Michael. Iron Catalyzed Hydroboration of Aldehydes and Ketones. Journal of Organic Chemistry, 2017. 82 (23): 12857-12862. doi:10.1021/acs.joc.7b02020
- ^ Alonso, Francisco; Candela, Pablo; Gomez, Cecilia; Yus, Miguel. The NiCl2-Li-arene (cat.) combination as reducing system, part 9: Catalytic hydrogenation of organic compounds using the NiCl2-Li-(naphthalene or polymer-supported naphthalene) (cat.) combination. Advanced Synthesis & Catalysis. 2003, 345 (1+2): 275-279. doi:10.1002/adsc.200390022.
- ^ Son, Eun-Kyung; Kang, Jae-Hyun; Kim, Deog-Bae; Kim, Jae-Hyun. Chemically amplified polymer having pendant group with dicyclohexyl for photoresist composition. PCT Int. Appl., 2004. WO 2004042477.
- ^ Montana, Angel M.; Barcia, Joan A.; Grima, Pedro M.; Kociok-Kohn, Gabriele. New methodology for the synthesis of tetrahydrofuro[3,2-b]furan-2(3H)-one derivatives, synthons of natural products with biological interest. Tetrahedron, 2016. 72 (43). 6794-6806. doi:10.1016/j.tet.2016.09.004