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| | (2-AMINO-6-CHLORO-PHENYL)-METHANOL Basic information |
| Product Name: | (2-AMINO-6-CHLORO-PHENYL)-METHANOL | | Synonyms: | (2-AMINO-6-CHLORO-PHENYL)-METHANOL;2-Amino-6-chlorobenzyl alcohol;2-Chloro-6-aminobenzyl alcohol;Benzenemethanol,2-amino-6-chloro-;2-Amino-6-chlorobenzenemethanol | | CAS: | 39885-08-0 | | MF: | C7H8ClNO | | MW: | 157.6 | | EINECS: | | | Product Categories: | | | Mol File: | 39885-08-0.mol |  |
| | (2-AMINO-6-CHLORO-PHENYL)-METHANOL Chemical Properties |
| Melting point | 76-78℃ | | Boiling point | 324.2±27.0 °C(Predicted) | | density | 1.341±0.06 g/cm3(Predicted) | | storage temp. | Keep in dark place,Inert atmosphere,Room temperature | | form | solid | | pka | 13.84±0.10(Predicted) | | color | White to off-white |
| | (2-AMINO-6-CHLORO-PHENYL)-METHANOL Usage And Synthesis |
| Synthesis | General procedure for the synthesis of (2-amino-6-chlorophenyl)-methanol from 2-amino-6-chlorobenzoic acid: 50.0 g (286 mmol) of 2-amino-6-chlorobenzoic acid was dissolved in 300 mL of anhydrous tetrahydrofuran (THF). The resulting solution was cooled to 0-10°C, followed by the slow addition of 450 mL of 1.0 M lithium aluminum hydride in THF solution. The reaction mixture was gradually warmed to room temperature and stirred continuously at room temperature overnight. Upon completion of the reaction, 300 mL of 10% aqueous sodium hydroxide solution was carefully added to the mixture to quench the reaction. The organic phase was separated and washed sequentially with ethyl acetate and water. The organic phase was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to remove the solvent, yielding 42 g (270 mmol, 95% yield) of a yellow solid product, which could be used without further purification. | | References | [1] Patent: CN107722059, 2018, A. Location in patent: Paragraph 0094; 0097; 0098; 0099
[2] Bioorganic and Medicinal Chemistry, 2012, vol. 20, # 19, p. 5810 - 5831
[3] Journal of Medicinal Chemistry, 2005, vol. 48, # 6, p. 2080 - 2092
[4] Patent: US2018/105527, 2018, A1. Location in patent: Paragraph 0783-0785
[5] Patent: WO2006/10142, 2006, A2. Location in patent: Page/Page column 70 |
| | (2-AMINO-6-CHLORO-PHENYL)-METHANOL Preparation Products And Raw materials |
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