Phthalimide
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| Names | |
|---|---|
| IUPAC name
Isoindole-1,3-dione | |
| Other names
1,3-dioxoisoindoline Phthalimidoyl (deprotonated) | |
| Identifiers | |
85-41-6  | |
| 3D model (Jmol) | Interactive image |
| ChEBI | CHEBI:38817 |
| ChEMBL | ChEMBL277294 |
| ChemSpider | 6550 |
| ECHA InfoCard | 100.001.458 |
| PubChem | 6809 |
| |
| |
| Properties[1] | |
| C8H5NO2 | |
| Molar mass | 147.13 g·mol−1 |
| Appearance | White solid |
| Melting point | 238 °C (460 °F; 511 K) |
| Boiling point | 336 °C (637 °F; 609 K) sublimes |
| <0.1 g/100 ml (19.5 °C) | |
| Acidity (pKa) | 8.3 |
| Basicity (pKb) | 5.7 |
| Related compounds | |
| Related Amides |
Maleimide |
| Related compounds |
Phthalic anhydride |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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| Infobox references | |
Phthalimide is the organic compound with the formula C6H4(CO)2NH. It is the imide derivative of phthalic anhydride. It is a sublimable white solid that is slightly soluble in water but more so upon addition of base. It is used as a precursor to other organic compounds as a masked source of ammonia.[2]
Preparation
Phthalimide can be prepared by heating phthalic anhydride with aqueous ammonia giving 95-97% yield. Alternatively, it may be prepared by treating the anhydride with ammonium carbonate or urea. It can also be produced by ammoxidation of ortho-xylene.[2]
Uses
Phthalimide is used as a precursor to anthranilic acid, a precursor to azo dyes and saccharin.[2]
Alkyl phthalimides are useful precursors to amines in chemical synthesis, especially in peptide synthesis where they are used "to block both hydrogens and avoid racemization of the substrates".[3] Alkyl halides can be converted to the N-alkylphthalimide:
- C6H4(CO)2NH + RX + NaOH → C6H4(CO)2N-R + NaX + H2O
The amine is commonly liberated using hydrazine:
- C6H4(CO)2NR + N2H4 → C6H4(CO)2N2H2 + RNH2
Dimethylamine can also be used.[4]
Some examples of Phthalimide drugs include Thalidomide, Amphotalide, Taltrimide & Talmetoprim.
Reactivity
It forms salts upon treatment with bases such as sodium hydroxide. The high acidity of the imido N-H is the result of the pair of flanking electrophilic carbonyl groups. Potassium phthalimide, made by reacting phthalimide with potassium carbonate in water at 100 °C or with potassium hydroxide in absolute ethanol,[5] is used in the Gabriel synthesis of primary amines, such as glycine.
Natural occurrence
Kladnoite is a natural mineral analog of phthalimide.[6] It is very rarely found among a few burning coal fire sites.
Safety
Phthalimide has low acute toxicity with LD50 (rat, oral) of greater than 5000 mg/kg.[2]
References
- ↑ "Phthalimide". Chemicalland21. Retrieved 15 November 2011.
- 1 2 3 4 Peter M. Lorz; Friedrich K. Towae; Walter Enke; Rudolf Jäckh; Naresh Bhargava; Wolfgang Hillesheim (2005), "Phthalic Acid and Derivatives", Ullmann's Encyclopedia of Industrial Chemistry, Weinheim: Wiley-VCH, doi:10.1002/14356007.a20_181.pub2
- ↑ "Phthalimides". Retrieved 2013-02-07.
- ↑ "DEPROTECTION – REMOVAL OF AMINE PROTECTING GROUPS (PHTHALIMIDE AND DIMETHYLAMINOSULPHONYL)". Retrieved 2013-02-07.
- ↑ "β-Bromoethylphthalimide". Organic Syntheses. Retrieved 15 November 2011.
- ↑ "Kladnoite". mindat.org. Retrieved 15 November 2011.
General reading (textbooks)
- Vollhardt, K. Peter C.; Schore, Neil Eric (2002). Organic Chemistry: Structure and Function (4th ed.). New York: W.H. Freeman. ISBN 978-0-7167-4374-3.
- Finar, Ivor Lionel (1973). Organic Chemistry. 1 (6th ed.). London: Longman. ISBN 0-582-44221-4.