4-Amino-2-nitro-benzoic acid ethyl ester

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4-Amino-2-nitro-benzoic acid ethyl ester Basic information
Product Name:4-Amino-2-nitro-benzoic acid ethyl ester
Synonyms:Benzoic acid, 4-amino-2-nitro-, ethyl ester;ETHYL 4-AMINO-2-NITROBENZOATE;4-Amino-2-nitro-benzoic acid ethyl ester
CAS:84228-46-6
MF:C9H10N2O4
MW:210.19
EINECS:
Product Categories:Aromatic Building Blocks;Aromatic Esters;API intermediates
Mol File:84228-46-6.mol
4-Amino-2-nitro-benzoic acid ethyl ester Structure
4-Amino-2-nitro-benzoic acid ethyl ester Chemical Properties
storage temp. Keep in dark place,Sealed in dry,Room Temperature
Safety Information
MSDS Information
4-Amino-2-nitro-benzoic acid ethyl ester Usage And Synthesis
Synthesis
Ethanol

64-17-5

CBI-BB ZERO/006118

21573-29-5

4-AMINO-2-NITRO-BENZOIC ACID ETHYL ESTER

84228-46-6

General steps: 1. dissolve 4-acetamido-2-nitrobenzoic acid (1.80 g, 8.0 mmol) in a mixture of 12 N hydrochloric acid (14 mL) and anhydrous ethanol (10 mL). 2. The reaction mixture was heated to 90-100°C and kept for 5 hours. 3. Upon completion of the reaction, the ethanol is removed by vacuum concentration. 4. The pH of the reaction mixture was adjusted to 4 with 1 N sodium hydroxide solution. 5. The precipitate was collected by filtration to give ethyl 4-amino-2-nitrobenzoate (140 mg, 8% yield). Product characterization data: 1H-NMR (CDCl3): δ 7.61 (d, J = 8.5 Hz, 1H), 6.82 (d, J = 2.1 Hz, 1H), 6.74 (dd, J = 8.5, 2.1 Hz, 1H), 6.52 (bs, 2H), 4.17 (q, J = 7.1 Hz, 2H), 1.21 (t, J = 7.1 Hz, 3H); MS ( DCI) m/e: 211 (MH+).

References[1] Patent: US5618839, 1997, A
[2] Patent: US5648385, 1997, A
4-Amino-2-nitro-benzoic acid ethyl ester Preparation Products And Raw materials
Raw materialsEthanol-->CBI-BB ZERO/006118-->Sodium hydroxide-->Hydrochloric acid
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