Carbazol-9-yl-methanol

Viktor, Milata; Rudolf, Kada; Ján, Lokaj

doi:10.3390/M354

Open AccessShort Note

Carbazol-9-yl-methanol

by

Milata Viktor

^1,*,

Kada Rudolf

¹ and

Lokaj Ján

²

¹

Department of Organic Chemistry Faculty of Chemical Technology, Slovak University of Technology, Radlinského 9, SK-812 37 Bratislava, Slovak Republic

²

Central Laboratory of Chemical Technique, Faculty of Chemical Technology, Slovak University of Technology, Radlinského 9, SK-812 37 Bratislava, Slovak Republic

^*

Author to whom correspondence should be addressed.

Molbank 2004, 2004(1), M354; https://doi.org/10.3390/M354

Submission received: 22 September 2003 / Accepted: 1 October 2003 / Published: 24 February 2004

Download Versions Notes

9H-Carbazole derivatives are known to have fluorescent properties and therefore they have exploitation in analytical chemistry, especially in bioanalytical chemistry. Carbazol-9-yl-methanol is a known agent in fluorescent analysis used with this aim.

Preparation of carbazol-9-yl-methanol is described only in patent literature [1] and in a journal difficult of access [2]. Title compound is stable only in alkaline alcoholic solutions and in acidic media turns to N,N´-biscarbazol-9-yl-methane [3].

To a mixture of carbazole (16,7 g, 0,1 mol) in ethanol (60 mL) is added potassium carbonate (10 g, 60 mmol) and the mixture is boiled under reflux for 5 min. with magnetic stirring. Then methanal (10 mL, 35 % aqueous solution, 0.1 mol) is added and heating is continued to dissolve all components. After next 10 min. the resulting reaction mixture is cooled, separated product is filtered off, dried and recrystallized from toluene. Yield 10.8 g ( 91.4 %).

M.p. 128-129 deg.C (toluene), 127-128 deg. C (EtOH) [1]; 128-129 deg. C (EtOH) [2].

TLC(CHCl₃/EtOH=9:1): R_f 0.57.

¹H NMR (DMSO-d₆, 300 MHz): 1.91t (1H, OH), 5.77d (2H,CH₂), 7.22t (1H,H-2), 7.45t (1H,H-3), 7.67d (1H,H-1,³J=8.4 Hz), 8.14d (1H,H-4,³J=7,8 Hz) ppm.

¹³C NMR (DMSO-d₆, 75 MHz): 65.33 (CH₂,¹J=55.11 Hz), 109.93 (C-1,C-8,¹J=163.17 Hz, ²J=9.06 Hz), 119.41 (C-3,C-6,¹J=161.16 Hz, ²J=8.06 Hz), 120.24 (C-4,C-5,¹J=160.15 Hz, ²J=8.06 Hz), 122.62 (C-4a, C-4b, ²J=5.8 Hz), 125.72 (C-2,C-7,¹J=161.15 Hz, ²J=7.05 Hz), 139.78 (C-8a, C-9a, ²J=4.3 Hz) ppm.

Anal. calc. for C₁₃H₁₁NO (197.24): C 79.17, H 5.62, N 7.10; found: C 79.01, H 5.66, N 7.24 %.

Supplementary materials

Supplementary File 1Supplementary File 2Supplementary File 3

Acknowledgements:

The authors would like to thank Slovak Grant Agency (financial support No. 1/9254/02 and 1/0058/03).

References and Notes

Lange, M. Ger. 256757 (1912). Chem. Abstr. 1913, 7, 2454. [Google Scholar]
Lopatinskii, V.P.; Sirotkina, E.E. Metody Poluch. Khim. Reakt. Prep. 1964, 88, Chem. Abstr. 1966, 64, 15823h.
Traven, V.F.; Smrček, V.A.; Stepanov, B.I. Khim. Geterotsikl. Soedin. 1967, 3, 568.

Share and Cite

MDPI and ACS Style

Viktor, M.; Rudolf, K.; Ján, L. Carbazol-9-yl-methanol. Molbank 2004, 2004, M354. https://doi.org/10.3390/M354

AMA Style

Viktor M, Rudolf K, Ján L. Carbazol-9-yl-methanol. Molbank. 2004; 2004(1):M354. https://doi.org/10.3390/M354

Chicago/Turabian Style

Viktor, Milata, Kada Rudolf, and Lokaj Ján. 2004. "Carbazol-9-yl-methanol" Molbank 2004, no. 1: M354. https://doi.org/10.3390/M354

APA Style

Viktor, M., Rudolf, K., & Ján, L. (2004). Carbazol-9-yl-methanol. Molbank, 2004(1), M354. https://doi.org/10.3390/M354

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Menu

Carbazol-9-yl-methanol

Supplementary materials

Acknowledgements:

References and Notes

Share and Cite

Article Metrics

Article Access Statistics

Further Information

Guidelines

MDPI Initiatives

Follow MDPI