1-乙炔基環己醇

1-乙炔基環己醇
識別
CAS號	78-27-3
SMILES	C#Cc1(O)ccccc1;
性質
化學式	C8H12O
摩爾質量	124.18 g·mol−1
密度	0.9809 g·cm−3（20 °C）
熔點	30 °C（303 K）; 31—32 °C（304—305 K）
沸點	179 °C（452 K）
	若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。

1-乙炔基環己醇是一種有機化合物，化學式為C₈H₁₂O，它可由乙炔和環己酮在氫氧化鉀的存在下於DMSO中反應製得。^[4]它和乙酸酐反應，生成乙酸-1-乙炔基環己酯。^[5]它和有機疊氮化物反應，乙炔基轉化為三唑。^[6]

參考文獻

^ Levina, R. Ya.; Vinogradova, E. I. Action of sodium acetylide on cyclic ketones. I. Synthesis of 1-ethynylcyclohexanol. Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation), 1936. 9: 1299-1302. ISSN: 0044-4618.
^ Verkruijsse, Hermann D.; Graaf, Wim de; Brandsma, Lambert. An Efficient and Quick Laboratory Scale Method for the Ethynylation of Some Aliphatic and Cycloaliphatic Carbonyl Compounds. Synthetic Communications. 1988, 18 (2): 131–134. ISSN 0039-7911. doi:10.1080/00397918808077336.
^ ^3.0 ^3.1 Nazarov, I. N.; Kotlyarevskii, I. L.; Ryabchenko, V. F. Acetylene derivatives. CLX. Condensation of aldehydes and ketones with acetylene under pressure. New method of synthesis of acetylenic alcohols. Zhurnal Obshchei Khimii, 1953. 23: 1900-1904. ISSN: 0044-460X.
^ Trofimov, B. A.; Sobenina, L. N.; Korostova, S. E.; Mikhaleva, A. I.; Shishov, N. I.; Fel'dman, V. D.; Shevchenko, S. G.; Vasil'ev, A. N. Synthesis of tertiary acetylenic alcohols and their ethers in a potassium hydroxide-dimethyl sulfoxide system. Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation), 1987. 60 (6): 1366-1370. ISSN: 0044-4618.
^ D'Elia, Valerio; Liu, Yinghao; Zipse, Hendrik. Immobilized DMAP Derivatives Rivaling Homogeneous DMAP. European Journal of Organic Chemistry. 2011, 2011 (8): 1527–1533. ISSN 1434-193X. doi:10.1002/ejoc.201001507.
^ Heriberto Díaz Velázquez, Yara Ruiz García, Matthias Vandichel, Annemieke Madder, Francis Verpoort. Water-soluble NHC-Cu catalysts: applications in click chemistry, bioconjugation and mechanistic analysis. Org. Biomol. Chem. 2014, 12 (46): 9350–9356 [2020-08-31]. ISSN 1477-0520. doi:10.1039/C4OB01350F （英語）.

[1] Levina, R. Ya.; Vinogradova, E. I. Action of sodium acetylide on cyclic ketones. I. Synthesis of 1-ethynylcyclohexanol. Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation), 1936. 9: 1299-1302. ISSN: 0044-4618.

[2] Verkruijsse, Hermann D.; Graaf, Wim de; Brandsma, Lambert. An Efficient and Quick Laboratory Scale Method for the Ethynylation of Some Aliphatic and Cycloaliphatic Carbonyl Compounds. Synthetic Communications. 1988, 18 (2): 131–134. ISSN 0039-7911. doi:10.1080/00397918808077336.

[Nazarov-3] 3.0 ^3.1 Nazarov, I. N.; Kotlyarevskii, I. L.; Ryabchenko, V. F. Acetylene derivatives. CLX. Condensation of aldehydes and ketones with acetylene under pressure. New method of synthesis of acetylenic alcohols. Zhurnal Obshchei Khimii, 1953. 23: 1900-1904. ISSN: 0044-460X.

[4] Trofimov, B. A.; Sobenina, L. N.; Korostova, S. E.; Mikhaleva, A. I.; Shishov, N. I.; Fel'dman, V. D.; Shevchenko, S. G.; Vasil'ev, A. N. Synthesis of tertiary acetylenic alcohols and their ethers in a potassium hydroxide-dimethyl sulfoxide system. Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation), 1987. 60 (6): 1366-1370. ISSN: 0044-4618.

[5] D'Elia, Valerio; Liu, Yinghao; Zipse, Hendrik. Immobilized DMAP Derivatives Rivaling Homogeneous DMAP. European Journal of Organic Chemistry. 2011, 2011 (8): 1527–1533. ISSN 1434-193X. doi:10.1002/ejoc.201001507.

[6] Heriberto Díaz Velázquez, Yara Ruiz García, Matthias Vandichel, Annemieke Madder, Francis Verpoort. Water-soluble NHC-Cu catalysts: applications in click chemistry, bioconjugation and mechanistic analysis. Org. Biomol. Chem. 2014, 12 (46): 9350–9356 [2020-08-31]. ISSN 1477-0520. doi:10.1039/C4OB01350F （英語）.

[1]

[2]

[3]

[4]

[5]

[6]