跳至內容

仙客來醛

本頁使用了標題或全文手工轉換
維基百科,自由的百科全書
仙客來醛
IUPAC名
3-(4-Isopropylphenyl)-2-methylpropanal
別名 兔耳草醛
對異丙基-α-甲基苯丙醛
對異丙基-α-甲基氫化肉桂醛
3-枯基異丁醛[1]
3-(4-異丙基苯基)-2-甲基丙醛
識別
CAS號 103-95-7  checkY
PubChem 517827
ChemSpider 451801
SMILES
 
  • CC(C)c1ccc(cc1)CC(C)C=O
性質
化學式 C13H18O
摩爾質量 190.28 g·mol−1
外觀 無色至淺黃色液體
氣味 強烈的花香
密度 0.947 g·cm−3[2]
沸點 104—105 °C(377—378 K)(3 mmHg)[2]
溶解性 難溶
溶解性(其它溶劑) 可溶於大部分混合油、乙醇;難溶於丙二醇丙三醇
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。

仙客來醛(英語:Cyclamen aldehyde)是一種有機化合物,化學式為C13H18O。仙客來醛具有山谷百合味香氣,其氣味及強度與間位異丙基的異構體相似[3],可用於香水製造[4]

合成

[編輯]

仙客來醛可由對異丙基-α-甲基肉桂醛在負載氧化鋁(或負載二氧化硅)的催化氫化得到。[5]β-甲基-4-異丙基苯丙醇被馬丁試劑氧化,也能製得仙客來醛。[6]

反應

[編輯]

仙客來醛和鹽酸羥胺四氯化鈦-吡啶體系中反應,可以得到α-甲基-4-異丙基苯丙腈,[7]羥胺-O-磺酸乙酸水溶液中也能完成這一轉化。[8]

它和4-硝基苯甲醛吡咯烷-乙酸催化下於二甲基亞碸中反應,經烯胺中間體,可以得到β-羥基-α-甲基-α-(4-異丙基苄基)-4-硝基苯丙醛。[9]

在催化下,它可以和乙二醇形成縮醛[10]

它和氟試劑乙酰丙酮亞鐵催化下於乙腈中反應,得到β-氟-α-甲基-4-異丙基苯丙醛(syn:anti=2:1)。[11]

參考文獻

[編輯]
  1. ^ 安家駒. 實用精細化工辭典. 中國輕工業出版社. 2000. ISBN 9787501927708.
  2. ^ 2.0 2.1 ABE, Shozou; YASUKAWA, Tadashi. Preparation of Cyclamen-type Perfume Compounds. I. Journal of Synthetic Organic Chemistry, Japan. 1964, 22 (2): 144–147 [2022-09-01]. ISSN 0037-9980. doi:10.5059/yukigoseikyokaishi.22.144. eISSN 1883-6526. (原始內容存檔於2022-09-01). 
  3. ^ Sell, C. S. On the Unpredictability of Odor. Angewandte Chemie International Edition. 25 September 2006, 45 (38): 6254–6261. ISSN 1433-7851. PMID 16983730. doi:10.1002/anie.200600782. eISSN 1521-3773. 
  4. ^ Danute Pajaujis Anonis. Lily of the Valley (Muguet) in Perfumery (PDF). Perfumer & flavorist. 1986, 11 (6): 31–36 [2022-09-03]. ISSN 0272-2666. (原始內容存檔 (PDF)於2022-09-03). CODEN PEFLDI
  5. ^ Pak, A. M.; Konuspaev, S. R.; Sagindykov, S. M.; Sokol'skii, D. V.; Zapletal, Vladimir; Prchlik, Jaroslav. Hydrogenation of forcyclamen- and forlilialaldehydes on supported metallic catalysts. Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation). 1986, 59 (5): 1135–1138. ISSN 0044-4618. CODEN ZPKHAB.
  6. ^ Limnios, Dimitris; Kokotos, Christoforos G. Microwave-assisted organocatalytic cross-aldol condensation of aldehydes. RSC Advances. 2013, 3 (14): 4496. doi:10.1039/c3ra00114h. eISSN 2046-2069. 
  7. ^ Leggio, Antonella; Belsito, Emilia Lucia; Gallo, Sonia; Liguori, Angelo. One-pot conversion of aldehydes to nitriles mediated by TiCl4. Tetrahedron Letters. April 2017, 58 (15): 1512–1514. ISSN 0040-4039. doi:10.1016/j.tetlet.2017.03.007. 
  8. ^ Quinn, Dylan J.; Haun, Graham J.; Moura-Letts, Gustavo. Direct synthesis of nitriles from aldehydes with hydroxylamine-O-sulfonic acid in acidic water. Tetrahedron Letters. August 2016, 57 (34): 3844–3847. ISSN 0040-4039. doi:10.1016/j.tetlet.2016.07.047. 
  9. ^ Mase, Nobuyuki; Tanaka, Fujie; Barbas, Carlos F. Rapid Fluorescent Screening for Bifunctional Amine−Acid Catalysts: Efficient Syntheses of Quaternary Carbon-Containing Aldols under Organocatalysis. Organic Letters. 24 October 2003, 5 (23): 4369–4372. ISSN 1523-7060. PMID 14602002. doi:10.1021/ol035651p. eISSN 1523-7052. 
  10. ^ Zou, Jianzhong; Yi, Fengping; Zhang, Lirong; Wang, Zhen. Facile Aldolization Catalyzed by Ionic Liquid [4-Sulfbmpyrazine][BF4]. Asian Journal of Chemistry. 2013, 25 (12): 6643–6646. ISSN 0970-7077. doi:10.14233/ajchem.2013.14396. eISSN 0975-427X. 
  11. ^ Bloom, Steven; Sharber, Seth Andrew; Holl, Maxwell Gargiulo; Knippel, James Levi; Lectka, Thomas. Metal-Catalyzed Benzylic Fluorination as a Synthetic Equivalent to 1,4-Conjugate Addition of Fluoride. The Journal of Organic Chemistry. 17 October 2013, 78 (21): 11082–11086. ISSN 0022-3263. PMID 24073747. doi:10.1021/jo401796g. eISSN 1520-6904.