Hu Ping-2

Molecules 2001, 6, M246

4-Ferrocenylbenzoic Acid

Ke-Qing Zhao*, Ping Hu and Hong-Bo Xu

Department of Chemistry, Sichuan Normal University, Chengdu, 610066, China
Tel./Fax: 86-28-4764743. Email: [email protected] (Present e-mail: [email protected])

Received: 28 May 2001 / Accepted: 14 December 2001 /Published: 20 December 2001

Keywords: Ferrocene, 4-aminobenzoic acid, 4-ferrocenylbenzoic acid, phase transfer catalysis, metallomesogen, intermediate, Gomberg-Bochmann reaction, arylation of ferrocene, hexadecyltrimethylammonium bromide

Ferrocene-containing liquid crystals, non-linear optical materials and magnetic materials are of considerable interests for their high thermal stability, tunable redox characteristics and structural variability [1]. 4-Ferrocenebenzoic acid is an important intermediate because it can be transferred into ester-type liquid crystal. The reported method of synthesis has very low yield [2]. We report a modified synthetic method using the reaction of ferrocene with diazonium salt of 4-aminobenzoic acid under the phase transfer catalysis. A mixture of 4-aminobenzoic acid (7.0 g, 50 mmol), 80 ml water, and 12 ml concentrated hydrochloric acid is cooled to 0-5°C with an ice-salt bath. A 20 ml aqueous solution of sodium nitrite (3.5g, 50 mmol) is added dropwise under stirring. After the addition is finished, it was stirred further for 30 min and the solution is kept in a temperature less than 5°C for use.

Ferrocene (10 g, 50 mmol) is dissolved in 100 ml ethyl ether, and 0.5 g hexadecyltrimethyl-ammonium bromide added and the mixture is cooled to 0-5°C under stirring. The above prepared diazonium salt solution is dropwise added with stirring. After addition is finished, it was further reacted 2 h in room temperature. Then ethyl ether is rotary evaporated to give red solid. The solid is dissolved in 500 ml water containing 5 g NaOH at 90°C and is filtrated while it was hot. The solid is the recovered, un-reacted ferrocene. The filtrate is cooled and the sodium salt of 4-ferrocenylbenzoic acid is precipitated. Filtration and acidification of the salt give 4-ferrocenylbenzoic acid as a red solid. Yield: 65%.

M.p., 240-241°C (decompose).

IR (KBr, cm^-1): 3200-2500, 1679, 1606, 1567, 1105, 1003.

¹HNMR: 4.02(s, 5H, C₅H₅), 4.3(s, 2H of C₅H₄), 4.7(s, 2H, C₅H₄), 7.2(d, 2H, C₆H₄), 7.9(d, 2H, C₆H₄).

Microanalysis for C₁₇H₁₄FeO₂: calculated, C, 66.61; H, 4.50%. Found: C, 66.67; H, 4.58%.

References

1. Togni, A.; Hayashi, T. Ferrocene; NewYork: VCH, 1994.
2.Weinmayr, V. J. Am. Chem. Soc. 1955, 77, 3012.

Sample Availability: Available from the authors and from MDPI.