Phthalic anhydride. II. The melting point of pure phthalic anhydride. the system: phthalic anhydride—phthalic acid

1920 ◽  
Vol 189 (1) ◽  
pp. 103-104
Author(s):  
K.P. Monroe
1972 ◽  
Vol 50 (11) ◽  
pp. 1675-1677 ◽  
Author(s):  
S. Jerumanis ◽  
P. A. Begin ◽  
D. Vu Cong

Catechol reacts with boron sulfide to give 2,2′-o-phenylenedioxybis-(1,3,2-benzodioxaborole) (1) while only the hydroxyl function of salicylic acid reacts to give a quantitative yield of tris(o-carboxylphenoxy)borane (3). Phthalic acid is dehydrated to phthalic anhydride, but succinic acid and maleic acid have been found inert to the action of the boron sulfide.


2014 ◽  
Vol 2014 ◽  
pp. 1-9
Author(s):  
Padam Praveen Kumar ◽  
Yervala Dathu Reddy ◽  
Chittireddy Venkata Ramana Reddy ◽  
Bhoomireddy Rama Devi ◽  
Pramod Kumar Dubey

Phthalic anhydride was treated with secondary amines in acetic acid yielding 2-(diethyl (or) 4-alkylpiperazine or morpholine-1-carbonyl) benzoic acids. The latter were reacted, again, with secondary amines and arylamines by using the coupling reagent HATU and Et3N as a base in DMF giving the novel symmetrical o-phthalic acid diamides [o-R1R1NCOC6H4CONR1R1], unsymmetrical o-phthalic acid diamides [o-R1R1NCOC6H4CONR1R2], and primary amidic-secondary amidic containing unsymmetrical o-phthalic acid diamides [o-R1R1NCOC6H4CONHAr], respectively.


1918 ◽  
Vol 10 (8) ◽  
pp. 596-598
Author(s):  
Charles R. Downs ◽  
Charles G. Stupp

Author(s):  
Bawa Kartar Singh ◽  
Kanwar Maghar Singh Manhas ◽  
Mahan Singh ◽  
Vimla Puri

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