Phthalimide

Phthalimide

Names
IUPAC name Isoindole-1,3-dione
Other names 1,3-dioxoisoindoline Phthalimidoyl (deprotonated)
Identifiers
CAS Number	85-41-6
3D model (Jmol)	Interactive image
ChEBI	CHEBI:38817
ChEMBL	ChEMBL277294
ChemSpider	6550
ECHA InfoCard	100.001.458
PubChem	6809
InChI InChI=1S/C8H5NO2/c10-7-5-3-1-2-4-6(5)8(11)9-7/h1-4H,(H,9,10,11) Key: XKJCHHZQLQNZHY-UHFFFAOYSA-N InChI=1/C8H5NO2/c10-7-5-3-1-2-4-6(5)8(11)9-7/h1-4H,(H,9,10,11) Key: XKJCHHZQLQNZHY-UHFFFAOYAS
SMILES O=C2c1ccccc1C(=O)N2
Properties[1]
Chemical formula	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
Solubility in water	<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

1. "Phthalimide". Chemicalland21. Retrieved 15 November 2011.
2. 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
3. "Phthalimides". Retrieved 2013-02-07.
4. "DEPROTECTION – REMOVAL OF AMINE PROTECTING GROUPS (PHTHALIMIDE AND DIMETHYLAMINOSULPHONYL)". Retrieved 2013-02-07.
5. "β-Bromoethylphthalimide". Organic Syntheses. Retrieved 15 November 2011.
6. "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.