3-AMINO-1,2-PHTHALIC ACID, DIMETHYL ESTER
3-AMINO-1,2-PHTHALIC ACID, DIMETHYL ESTER Basic information
- Product Name:
- 3-AMINO-1,2-PHTHALIC ACID, DIMETHYL ESTER
- Synonyms:
-
- 3-AMINO-1,2-PHTHALIC ACID, DIMETHYL ESTER
- 3-Amino-phthalic acid dimethyl ester
- 3-aminobenzene-1,2-dicarboxylic acid dimethyl ester
- 3-Amino-1,2-benzenedicarboxylic acid 1,2-dimethyl ester
- dimethyl 3-aminophthalate
- Methyl 3-amino-2-(methoxycarbonyl)benzoate
- 1,2-diMethyl 3-aMinobenzene-1,2-dicarboxylate
- 1,2-Benzenedicarboxylicacid, 3-aMino-, 1,2-diMethyl ester
- CAS:
- 34529-06-1
- MF:
- C10H11NO4
- MW:
- 209.2
- EINECS:
- 200-258-5
- Mol File:
- 34529-06-1.mol
3-AMINO-1,2-PHTHALIC ACID, DIMETHYL ESTER Chemical Properties
- Boiling point:
- 306℃
- Density
- 1.248
- Flash point:
- 136℃
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- pka
- 1.05±0.10(Predicted)
- Appearance
- Off-white to yellow Solid-Liquid Mixture
3-AMINO-1,2-PHTHALIC ACID, DIMETHYL ESTER Usage And Synthesis
Uses
Dimethyl 3-aminophthalate is a useful research chemical.
Synthesis
13365-26-9
34529-06-1
The general procedure for the synthesis of dimethyl 3-amino-phthalate from methyl 3-nitrophthalate was as follows: first, methyl 3-nitrophthalate was converted to the corresponding chloride by a chlorination reaction, followed by esterification to obtain dimethyl 3-nitrophthalate (100% yield). Next, the nitro group was reduced to an amino group by catalytic hydrogenation to obtain dimethyl 3-amino-phthalate (100% yield). Subsequently, diazotization of the amino group was followed by iodination to obtain dimethyl 3-iodophthalate (about 91% yield). Then, a saponification reaction was carried out on dimethyl 3-iodophthalate, followed by acidification to obtain 3-iodophthalic acid (yield about 93%). Finally, 3-iodophthalic acid was oxidized and reacted in the presence of KBrO3 and 0.73 M H2SO4 at 55-60 °C for 12 h to obtain water-soluble MIBX.Upon completion of the reaction, purification by evaporation, cooled milling and filtration yielded white solid MIBX (~70% yield, melting point 258-260 °C). The conversion of the process is nearly quantitative and can be monitored by 1H NMR spectroscopy.The physical properties of MIBX include IR (KBr) showing characteristic absorption peaks; 1H NMR (D2O, 300 MHz) and 13C NMR (D2O, 75 MHz) showing specific chemical shifts.
References
[1] Journal of Heterocyclic Chemistry, 1989, vol. 26, # 6, p. 1885 - 1886
[2] Tetrahedron Letters, 2002, vol. 43, # 4, p. 569 - 572
[3] Patent: US2004/30187, 2004, A1. Location in patent: Page 2; Sheet 1
[4] RSC Advances, 2015, vol. 5, # 60, p. 48861 - 48867
[5] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 1, p. 285 - 288
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