Nadic anhydride

Nadic anhydride
endo	exo
Names
	Systematic IUPAC name 24-oxatricyclo[5.2.1.02,6]dec-8-ene-3,5-dione
	Other names 5-Norbornene-2,3-dicarboxylic anhydride; Nadic acid anhydride; Himic anhydride (exo); Carbic anhydride (endo)
Identifiers
CAS Number	826-62-0 ; 2746-19-2 (exo) ; 129-64-6 (endo) ;
3D model (JSmol)	Interactive image;
ChemSpider	12668 ;
EC Number	212-557-9;
PubChem CID	13223;
	InChI InChI=1S/C9H8O3/c10-8-6-4-1-2-5(3-4)7(6)9(11)12-8/h1-2,4-7H,3H2 Key: KNDQHSIWLOJIGP-UHFFFAOYSA-N ; InChI=1S/C9H8O3/c10-8-6-4-1-2-5(3-4)7(6)9(11)12-8/h1-2,4-7H,3H2 Key: KNDQHSIWLOJIGP-UHFFFAOYSA-N;
	SMILES C1C2C=CC1C3C2C(=O)OC3=O;
Properties
Chemical formula	C9H8O3
Molar mass	164.160 g·mol−1
Appearance	white solid
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Nadic anhydride, also known as 5-norbornene-2,3-dicarboxylic anhydride, is an organic acid anhydride derivative of norbornene.

Stereochemistry

Nadic anhydride exhibits endo-exo isomerism. In the exo isomer, the acid anhydride group points in the same direction towards the bridging carbon of the norbornene, while in the endo isomer the acid anhydride group points in the opposite direction. These isomers are respectively named cis-5-norbornene-exo-2,3-dicarboxylic anhydride (also known as himic anhydride) and cis-5-norbornene-endo-2,3-dicarboxylic anhydride (also known as carbic anhydride).^[1]^[2] Commercially available nadic anhydride is mainly the endo isomer, as this is the isomer predominantly made in the Diels-Alder reaction in its synthesis.^[3]



endo	exo

Preparation

In the patent for the Diels-Alder reaction, nadic anhydride was given as an example of the reaction, made by the condensation of maleic anhydride and cyclopentadiene, which gives mostly the endo isomer.^[3] The endo isomer can be converted into the exo isomer by irradiation with UV light.^[4]

Uses

Due to the reactivity of the norbornene moiety in the thiol-ene reaction, nadic anhydride is used in the synthesis of monomers for cross-linked polymer networks based on thiol-ene linkages.^[5]

References

↑ Template:Cite PubChem
↑ Template:Cite PubChem
↑ ^3.0 ^3.1 & Kurt Alder"Organic compound having hydrogenated ring systems and process of preparing it" StatesUS1944731A United States patent US1944731A, published January 23, 1934
↑ Pandey, Bipin; Athawale, Asawar A.; Reddy, Ravinder S.; Dalvi, Pravinder S.; Kumar, Pradeep (1991). "A Remarkably Efficient Photochemical Methodology for Endo to Exo IsomerizatLon of Dials–Alder Cycloadducts". Chemistry Letters 20 (7): 1173–1176. doi:10.1246/cl.1991.1173.
↑ Hoyle, Charles E.; Bowman, Christopher N. (2010). "Thiol–Ene Click Chemistry". Angewandte Chemie International Edition 49 (9): 1540–1573. doi:10.1002/anie.200903924.

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[1] Template:Cite PubChem

[2] Template:Cite PubChem

[dielsalder-3] 3.0 ^3.1 & Kurt Alder"Organic compound having hydrogenated ring systems and process of preparing it" StatesUS1944731A United States patent US1944731A, published January 23, 1934

[4] Pandey, Bipin; Athawale, Asawar A.; Reddy, Ravinder S.; Dalvi, Pravinder S.; Kumar, Pradeep (1991). "A Remarkably Efficient Photochemical Methodology for Endo to Exo IsomerizatLon of Dials–Alder Cycloadducts". Chemistry Letters 20 (7): 1173–1176. doi:10.1246/cl.1991.1173.

[5] Hoyle, Charles E.; Bowman, Christopher N. (2010). "Thiol–Ene Click Chemistry". Angewandte Chemie International Edition 49 (9): 1540–1573. doi:10.1002/anie.200903924.

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Nadic anhydride

Topic: Chemistry

Contents

Stereochemistry

Preparation

Uses

References