Sen, A. B. published the artcileOrganic fungicides. IV. Preparation of some aryloxy-fatty acids and their mercury derivatives, COA of Formula: C12H16O3, the publication is Journal of the Indian Chemical Society (1951), 469-70, database is CAplus.
The aryloxy aliphatic acids were prepared by heating the appropriate phenol (1 mol.), the halogenated fatty acid (1 mol.) and NaOH (2 mols.) at 100¡ã for 3-6 h., and either crystallized from 10% MeOH or petr. ether or distilled in vacuo. The following acids are reported: 4-EtC6H4OCH2CO2h (I) m. 91¡ã; 3-EtC6H4OCH2CO2H (II), m. 73¡ã; 4-Me3CC6H4OCH2CO2H (III), m. 80¡ã; 4-Me2(Et)CC6H4OCH2CO2H (IV), m. 50¡ã; 4-EtC6H4OCH2CH2CO2H (V), m. 50¡ã; 3-EtC6H4OCH2CH2CO2H (VI), m. 51¡ã, b12 188¡ã; 4-Me3CC6H4OCH2CH2CO2H (VII), m. 51-2¡ã; 4-Me2(Et)CC6H4OCH2CH2CO2H (VIII), b3 210¡ã; 4-Me3CC6H4O(CH2)3CO2H (IX), 84, b20 210¡ã; 4-Me2(Et)CC6H4O(CH2)3CO2H (X), m. 54¡ã, b18 198¡ã. Equimol. amounts Hg(OAc)2 in H2O and the aryloxy aliphatic acids in dilute AcOH, or HgO in 50% AcOH and the aryloxy aliphatic acid in 50% alc. were heated 1-6 h. on a steam bath until a sandy powder separated ((RCO2)2Hg compound corresponding to the above acids and m.p.): I, 224¡ã (with decomposition); II, 198¡ã (with decomposition); III, 192¡ã; IV, 160¡ã; V, 227¡ã; VI, 234¡ã (with decomposition); VII, 248¡ã (with decomposition); VIII, 228¡ã; IX, 238¡ã (with decomposition); and X, 240¡ã (with decomposition).
Journal of the Indian Chemical Society published new progress about 1798-04-5. 1798-04-5 belongs to catalysis-chemistry, auxiliary class Carboxylic acid,Benzene,Ether, name is 2-(4-(tert-Butyl)phenoxy)acetic acid, and the molecular formula is C3H8N2S, COA of Formula: C12H16O3.
Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia