An Efficient Procedure for Microscale Synthesis of Semicarbazones

*[email protected]. (1–3). The following carbonyl compounds were converted to semicarbazones by the grinding procedure: benzaldehyde...
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In the Laboratory

An Efficient Procedure for Microscale Synthesis of Semicarbazones Sangeeta Pandita,* Samta Goyal, Nadira Arif, and Sarita Passey Department of Chemistry, Zakir Husain College, J. L. Nehru Marg, New Delhi 110-002, India; *[email protected]

Semicarbazones are useful derivatives to identify and characterize carbonyl compounds (1, 2). The following experimental grinding procedure is useful in identifying several carbonyl compounds. Semicarbazide hydrochloride (100 mg, 1 mmole) and sodium acetate (100 mg) are placed in a mortar and ground with a pestle (Scheme I). After the mixture turns to liquid, a carbonyl compound (1 mmole) is added. Grinding is continued for several minutes until a smooth paste is formed. The crude semicarbazone separates on addition of cold water to the paste and is recrystallized from ethanol. The crystallized product is vacuum filtered using a glass funnel and a Willstätter nail (1). Complete drying occurs in ∼5 minutes. The melting point of the purified semicarbazones is compared to those found in the literature

(1–3). The following carbonyl compounds were converted to semicarbazones by the grinding procedure: benzaldehyde 2-nitrobenzaldehyde 4-nitrobenzaldehyde 2,4-dichlorobenzaldehyde 3-bromobenzaldehydenaphthalene-1-carbaldehyde 4-hydroxybenzaldehyde acetophenone 4-bromoacetophenone 4-nitroacetophenone 4-hydroxyacetophenone 1-acetylnaphthalene 2-butanone 4-methyl-2-butanone

O C H2N

N NH2 H ⭈HCl

2-pentanone

O

+

C H3C

OⴚNaⴙ

Semicarbazide hydrochloride (CAS #563-41-7) is harmful if swallowed, inhaled, or absorbed through skin. Protective lab equipment should be worn during the synthesis procedure.

grinding

O C R

Literature Cited

R'

1. Vogel, A. I. Text book of Practical Organic Chemistry, 4th ed.; ELBS: Longman, U.K., 1978. 2. Cheronis, N. D ; Entrikin, J. B.; Hodnett, E. M. Semimicro Qualitative Organic Analysis; Interscience Publishers: New York, 1965. 3. Kolb, V. M.; Stupar, J. W.; Janota, T. E.; Duax, W. L. J. Org. Chem. 1989, 54, 2341.

O R'

C C

R

N

N H

NH2

Scheme I. Reaction to form semicarbazones.

108

Journal of Chemical Education

Hazards



Vol. 81 No. 1 January 2004



www.JCE.DivCHED.org