cas 16110-99-9, 3,6-dichlorophthalic acid | Articles data

Articles about 16110-99-9Total 3 be found

Optimization of Reaction Variables in the Selective Hydrodechlorination of Chlorinated Phthalic Anhydrides and Acids: Preparation of 3,6-Dichlorophthalic Acid and 3-Chlorophthalic Acid
-
Fertel, Lawrence B.,O'Reilly, Neil J.,Callaghan, Kathleen M.
p. 261 - 263
(1993)
Read Online

Synthetic method
A process for the preparation of the compound AQ4 of formula 3: or a salt or N-oxide thereof, includes the step:
-
(2008/06/13)

A large-scale synthesis of the bioreductive drug 1,4-bis{[2-(dimethylamino)ethyl]amino}-5,8-dihydroxyanthracene-9,10-dione bis-N-oxide (AQ4N)
A large-scale synthesis of the bis-bioreductive drug 1,4-bis{[2-(dimethylamino)ethyl]amino}-5,8-dihydroxy-anthracene-9,10-dione bis-N-oxide (AQ4N) has been developed. This six-step synthesis provides AQ4N in 20% overall yield from readily available tetrachlorophthalic anhydride. The key step was a KF-NaF-mediated conversion of 3,6-dichlorophthalic anhydride to 3,6-difluorophthalic anhydride, which could be achieved in 77% yield on a 100 g scale. A trace impurity in AQ4N was determined (by LC-MS and independent synthesis) to be the mono-N-oxide 1-amino-4-[2-(dimethylamino)ethyl]amino-5,8-dihydroxyanthracene-9,10-dione N-oxide. This is formed spontaneously from AQ4N under a number of conditions, including during HPLC on reversed-phase columns. The Royal Society of Chemistry 1999.
Lee, Ho H.,Denny, William A.
p. 2755 - 2758
(2007/10/03)