2-丙烯基-4-甲氧基苯酚

Pseudoisoeugenol
	IUPAC名; 4-Methoxy-2-[(1E)-prop-1-en-1-yl]phenol
別名	2-(1-Propenyl)-4-methoxyphenol; trans-Pseudoisoeugenol
識別
CAS號	17398-03-7 ; 98755-22-7（1E）
PubChem	16116489
ChemSpider	17273716
SMILES	CC=CC1=C(C=CC(=C1)OC)O;
InChI	1S/C10H12O2/c1-3-4-8-7-9(12-2)5-6-10(8)11/h3-7,11H,1-2H3/b4-3+;
InChIKey	CNTCZYAGRDSWBW-ONEGZZNKSA-N
性質
化學式	C10H12O2
摩爾質量	164.2 g·mol−1
密度	1.0 g/cm3
沸點	357.3 °C（630 K）
	若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。

2-丙烯基-4-甲氧基苯酚是天然存在的苯丙烯類化合物，化學式為C₁₀H₁₂O₂，它是丁香油酚和異丁香油酚的同分異構體。^[1]它可以2-羥基-5-甲氧基苯甲醛為原料反應得到，^[2]或通過2-烯丙基-4-甲氧基苯酚的異構化製得。^[3]它和烯丙基二甲基氯硅烷在三乙胺存在下反應，可以得到3-丙烯基-4-(烯丙基二甲基硅氧基)苯甲醚。^[4]

參考文獻[編輯]

^ Reichling, Jürgen; Galati, Enza Maria. Jodral, Manuel Miró , 編. Illicium, Pimpinella and Foeniculum 1st. New York: CRC Press LLC. 2004: 79–90 [2022-03-09]. ISBN 9780203022320. （原始內容存檔於2022-03-09）.
^ Ehu Camille Aka, Eric Wimmer, Elvina Barré, Natarajan Vasudevan, Daniel Cortés-Borda, Tchirioua Ekou, Lynda Ekou, Mireia Rodriguez-Zubiri, François-Xavier Felpin. Reconfigurable Flow Platform for Automated Reagent Screening and Autonomous Optimization for Bioinspired Lignans Synthesis. The Journal of Organic Chemistry. 2019-11-01, 84 (21): 14101–14112 [2022-03-09]. ISSN 0022-3263. doi:10.1021/acs.joc.9b02263. （原始內容存檔於2022-02-25）（英語）.
^ Tuyen Nguyen Van, Silvia Debenedetti, Norbert De Kimpe. Synthesis of coumarins by ring-closing metathesis using Grubbs’ catalyst. Tetrahedron Letters. 2003-05, 44 (22): 4199–4201 [2022-03-09]. doi:10.1016/S0040-4039(03)00902-X. （原始內容存檔於2018-06-18）（英語）.
^ Leticia Jiménez-González, Sergio García-Muñoz, Miriam Álvarez-Corral, Manuel Muñoz-Dorado, Ignacio Rodríguez-García. Silver-Catalyzed Asymmetric Synthesis of 2,3-Dihydrobenzofurans: A New Chiral Synthesis of Pterocarpans. Chemistry - A European Journal. 2006-11-24, 12 (34): 8762–8769 [2022-03-09]. doi:10.1002/chem.200600332 （英語）.

[Reichling-1] Reichling, Jürgen; Galati, Enza Maria. Jodral, Manuel Miró , 編. Illicium, Pimpinella and Foeniculum 1st. New York: CRC Press LLC. 2004: 79–90 [2022-03-09]. ISBN 9780203022320. （原始內容存檔於2022-03-09）.

[2] Ehu Camille Aka, Eric Wimmer, Elvina Barré, Natarajan Vasudevan, Daniel Cortés-Borda, Tchirioua Ekou, Lynda Ekou, Mireia Rodriguez-Zubiri, François-Xavier Felpin. Reconfigurable Flow Platform for Automated Reagent Screening and Autonomous Optimization for Bioinspired Lignans Synthesis. The Journal of Organic Chemistry. 2019-11-01, 84 (21): 14101–14112 [2022-03-09]. ISSN 0022-3263. doi:10.1021/acs.joc.9b02263. （原始內容存檔於2022-02-25）（英語）.

[3] Tuyen Nguyen Van, Silvia Debenedetti, Norbert De Kimpe. Synthesis of coumarins by ring-closing metathesis using Grubbs’ catalyst. Tetrahedron Letters. 2003-05, 44 (22): 4199–4201 [2022-03-09]. doi:10.1016/S0040-4039(03)00902-X. （原始內容存檔於2018-06-18）（英語）.

[4] Leticia Jiménez-González, Sergio García-Muñoz, Miriam Álvarez-Corral, Manuel Muñoz-Dorado, Ignacio Rodríguez-García. Silver-Catalyzed Asymmetric Synthesis of 2,3-Dihydrobenzofurans: A New Chiral Synthesis of Pterocarpans. Chemistry - A European Journal. 2006-11-24, 12 (34): 8762–8769 [2022-03-09]. doi:10.1002/chem.200600332 （英語）.

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