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| | methyl 3-amino-5-chlorobenzoate Basic information |
| Product Name: | methyl 3-amino-5-chlorobenzoate | | Synonyms: | methyl 3-amino-5-chlorobenzoate;Benzoic acid, 3-aMino-5-chloro-, Methyl ester;Methyl3-amino-5-chlorobenzoate98%;3-AMINO-5-CHLORO-BENZOIC ACID METHYL ESTER;Methyl 3-amino-5-chlorobenzoate 98% | | CAS: | 21961-31-9 | | MF: | C8H8ClNO2 | | MW: | 185.61 | | EINECS: | | | Product Categories: | | | Mol File: | 21961-31-9.mol |  |
| | methyl 3-amino-5-chlorobenzoate Chemical Properties |
| Boiling point | 329.4±22.0 °C(Predicted) | | density | 1.311±0.06 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2–8 °C | | pka | 2.39±0.10(Predicted) | | Appearance | White to yellow Solid |
| | methyl 3-amino-5-chlorobenzoate Usage And Synthesis |
| Synthesis | Step 2: Synthesis of methyl 3-amino-5-chlorobenzoate
A dioxane solution (0.13 M) of methyl 3-chloro-5-nitrobenzoate (from Step 1) was placed in a reaction flask and SnCl2 (3.9 equiv) was added. The reaction mixture was stirred at 70 °C for 2 hours. After completion of the reaction, it was cooled to room temperature and EtOAc and saturated aqueous NaHCO3 solution was added. The reaction mixture was filtered to remove the precipitate formed. The aqueous phase was separated and extracted with EtOAc. All organic layers were combined and dried with anhydrous Na2SO4. Evaporation of the solvent under reduced pressure afforded the title compound methyl 3-amino-5-chlorobenzoate in 88% yield as a yellow solid. Mass spectrum (ES+) m/z 186,188 (M+H)+. | | References | [1] Patent: WO2007/28789, 2007, A1. Location in patent: Page/Page column 35
[2] Patent: US2010/261687, 2010, A1. Location in patent: Page/Page column 60 |
| | methyl 3-amino-5-chlorobenzoate Preparation Products And Raw materials |
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