METHYL 2-AMINO-5-METHYLBENZOATE
METHYL 2-AMINO-5-METHYLBENZOATE Basic information
- Product Name:
- METHYL 2-AMINO-5-METHYLBENZOATE
- Synonyms:
-
- METHYL 2-AMINO-5-METHYLBENZOATE
- Methyl 5-methylanthranilate
- [2-(Methoxycarbonyl)phenyl]aMine
- NSC 3109
- o-(Methoxycarbonyl)aniline
- SunaroMe UVA
- 5-Methyl-2-aMinobenzoic acid Methyl ester
- 2-Amino-5-methylbenzoic acid methyl ester
- CAS:
- 18595-16-9
- MF:
- C9H11NO2
- MW:
- 165.19
- Product Categories:
-
- Aromatics Compounds
- Aromatics
- Mol File:
- 18595-16-9.mol
METHYL 2-AMINO-5-METHYLBENZOATE Chemical Properties
- Melting point:
- 54-56°C
- Density
- 1.132
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- solubility
- Dichloromethane, Ethyl Acetate, Methanol
- form
- Solid
- color
- Yellow to Brown
METHYL 2-AMINO-5-METHYLBENZOATE Usage And Synthesis
Chemical Properties
METHYL 2-AMINO-5-METHYLBENZOATE is yellow Solid
Uses
METHYL 2-AMINO-5-METHYLBENZOATE is a useful synthetic intermediate
Uses
A useful synthetic intermediate.
Synthesis
20587-30-8
18595-16-9
Methyl 5-methyl-2-nitrobenzoate (8 g, 41.025 mmol) was used as a raw material in a solvent mixture of methanol (80 mL) and water (10 mL), and cooled to 0 °C. Subsequently, zinc powder (13.33 g, 205.128 mmol) and NH4Cl (17.6 g, 328.2 mmol) were added sequentially. The reaction mixture was stirred at room temperature for 12 h. The reaction progress was monitored by TLC (unfolding agent: 20% ethyl acetate/hexane). After completion of the reaction, the mixture was filtered and the filtrate was evaporated to give the crude product. The crude product was alkalized with saturated NaHCO3 solution and extracted with dichloromethane (2 x 20 mL). The organic layers were combined, dried with Na2SO4, filtered and the solvent was evaporated to give the target compound methyl 2-amino-5-methylbenzoate (yield: 4 g, 60%).1H NMR (400 MHz, CDCl3) data were as follows: δ 7.65 (s, 1H), 7.25 (s, 1H), 7.10-7.07 (q, 1H, J=8Hz), 6.58 (d, 1H), 3.86 (s, 3H), 2.22 (s, 3H).
References
[1] Patent: WO2015/38417, 2015, A1. Location in patent: Paragraph 151; 152
[2] Journal of the Chemical Society, 1930, p. 1513,1516
[3] Bioorganic and Medicinal Chemistry Letters, 2009, vol. 19, # 15, p. 4416 - 4420
[4] Patent: EP1475368, 2004, A1. Location in patent: Page 57
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