4-叔丁基-1,2-苯二酚

4-tert-Butylcatechol
	IUPAC名; 4-tert-Butylbenzene-1,2-diol
別名	4-叔丁基鄰苯二酚; 對叔丁基鄰苯二酚
識別
縮寫	TBC
CAS號	98-29-3
PubChem	7381
ChemSpider	7103
SMILES	Oc1ccc(cc1O)C(C)(C)C;
InChI	1/C10H14O2/c1-10(2,3)7-4-5-8(11)9(12)6-7/h4-6,11-12H,1-3H3;
InChIKey	XESZUVZBAMCAEJ-UHFFFAOYAR
性質
化學式	C10H14O2
摩爾質量	166.217 g·mol⁻¹
熔點	54 °C（327 K）
沸點	285 °C（558 K）
	若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。

4-叔丁基-1,2-苯二酚是一種有機化合物，化學式為C₁₀H₁₄O₂。它可由鄰苯二酚和2-甲基丙烯加熱反應製得。^[3]它和NBS反應，可以得到3-溴-5-叔丁基-1,2-苯二酚^[4]；它可以被高碘酸鈉氧化為4-叔丁基-3,5-環己二烯-1,2-二酮^[5]。它可用作烯烴的阻聚劑和抗氧化劑。^[6]

參考文獻

^ Yasuhiro Kamitori, Masaru Hojo, Ryoichi Masuda, Tatsuo Izumi, Shuichi Tsukamoto. Silica gel as an effective catalyst for the alkylation of phenols and some heterocyclic aromatic compounds. The Journal of Organic Chemistry. 1984-11, 49 (22): 4161–4165 [2020-05-29]. ISSN 0022-3263. doi:10.1021/jo00196a012 （英語）.
^ "PhysProp" data were obtained from Syracuse Research Corporation of Syracuse, New York (US). Retrieved from SciFinder. [2020-5-17]
^ 楊春華, 劉凌波, 臧陽陵,等. 對叔丁基鄰苯二酚的合成研究. 精細化工中間體, 2007, 037(003):25-26,62. doi: CNKI:SUN:HNHG.0.2007-03-007
^ Kevin Greenaway, Paolo Dambruoso, Alessandro Ferrali, Andrew Hazelwood, Filippo Sladojevich, Darren Dixon. Enantioselective Organocatalytic Aryloxylation of β-Keto Esters. Synthesis. 2011-06, 2011 (12): 1880–1886 [2020-05-29]. ISSN 0039-7881. doi:10.1055/s-0030-1260059. （原始內容存檔於2018-06-05）（英語）.
^ Annika Borrmann, Olumide Fatunsin, Jan Dommerholt, Anika M. Jonker, Dennis W. P. M. Löwik, Jan C. M. van Hest, Floris L. van Delft. Strain-Promoted Oxidation-Controlled Cyclooctyne–1,2-Quinone Cycloaddition (SPOCQ) for Fast and Activatable Protein Conjugation. Bioconjugate Chemistry. 2015-02-18, 26 (2): 257–261 [2020-05-29]. ISSN 1043-1802. doi:10.1021/bc500534d. （原始內容存檔於2020-11-21）（英語）.
^ 對叔丁基鄰苯二酚（頁面存檔備份，存於互聯網檔案館）. ChemicalBook. [2020-05-17].

[1] Yasuhiro Kamitori, Masaru Hojo, Ryoichi Masuda, Tatsuo Izumi, Shuichi Tsukamoto. Silica gel as an effective catalyst for the alkylation of phenols and some heterocyclic aromatic compounds. The Journal of Organic Chemistry. 1984-11, 49 (22): 4161–4165 [2020-05-29]. ISSN 0022-3263. doi:10.1021/jo00196a012 （英語）.

[2] "PhysProp" data were obtained from Syracuse Research Corporation of Syracuse, New York (US). Retrieved from SciFinder. [2020-5-17]

[3] 楊春華, 劉凌波, 臧陽陵,等. 對叔丁基鄰苯二酚的合成研究. 精細化工中間體, 2007, 037(003):25-26,62. doi: CNKI:SUN:HNHG.0.2007-03-007

[4] Kevin Greenaway, Paolo Dambruoso, Alessandro Ferrali, Andrew Hazelwood, Filippo Sladojevich, Darren Dixon. Enantioselective Organocatalytic Aryloxylation of β-Keto Esters. Synthesis. 2011-06, 2011 (12): 1880–1886 [2020-05-29]. ISSN 0039-7881. doi:10.1055/s-0030-1260059. （原始內容存檔於2018-06-05）（英語）.

[5] Annika Borrmann, Olumide Fatunsin, Jan Dommerholt, Anika M. Jonker, Dennis W. P. M. Löwik, Jan C. M. van Hest, Floris L. van Delft. Strain-Promoted Oxidation-Controlled Cyclooctyne–1,2-Quinone Cycloaddition (SPOCQ) for Fast and Activatable Protein Conjugation. Bioconjugate Chemistry. 2015-02-18, 26 (2): 257–261 [2020-05-29]. ISSN 1043-1802. doi:10.1021/bc500534d. （原始內容存檔於2020-11-21）（英語）.

[6] 對叔丁基鄰苯二酚（頁面存檔備份，存於互聯網檔案館）. ChemicalBook. [2020-05-17].

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