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| 5-AMino-2,4-di-tert-butylphenol Basic information |
Product Name: | 5-AMino-2,4-di-tert-butylphenol | Synonyms: | 5-AMino-2,4-di-tert-butylphenol;2,4-Di-tert-butyl-5-aMinophenyl Methyl carbonate;Phenol, 5-amino-2,4-bis(1,1-dimethylethyl)-;5-Amino-2,4-bis(2-methyl-2-propanyl)phenol;VX-770 intermediate;5-amino-2,4-di-tert-butylphenol hydrochloride (base);4,6-dichloropyridazin-4-ol;5-Amino-2,4-ditertiarybutyphenol | CAS: | 873055-58-4 | MF: | C14H23NO | MW: | 221.34 | EINECS: | | Product Categories: | | Mol File: | 873055-58-4.mol | |
| 5-AMino-2,4-di-tert-butylphenol Chemical Properties |
Boiling point | 319.7±30.0 °C(Predicted) | density | 0.990±0.06 g/cm3(Predicted) | storage temp. | 2-8°C(protect from light) | pka | 11.63±0.23(Predicted) | InChI | InChI=1S/C14H23NO/c1-13(2,3)9-7-10(14(4,5)6)12(16)8-11(9)15/h7-8,16H,15H2,1-6H3 | InChIKey | BKSDHPHOWDUJNB-UHFFFAOYSA-N | SMILES | C1(O)=CC(N)=C(C(C)(C)C)C=C1C(C)(C)C |
| 5-AMino-2,4-di-tert-butylphenol Usage And Synthesis |
Uses | 5-Amino-2,4-di-tert-butylphenol is an intermediate used in the preparation of ivacaftor via condensation of oxo dihydroquinoline carboxylic acid with amino ditert butylphenol. | Synthesis | To a refluxing solution of 2,4-di-tert-butyl-5-nitro-phenol (1.86 g, 7.40 mmol) and ammonium formate (1.86 g) in ethanol (75 mL) was added Pd-5% wt on activated carbon (900 mg). The reaction mixture was stirred at reflux for 2 h, cooled to room temperature, and filtered through Celite. The Celite was washed with methanol, and the combined filtrates were concentrated to yield 5-amino-2,4-di-tert-butyl-phenol as a grey solid (1.66 g, quant.).
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| 5-AMino-2,4-di-tert-butylphenol Preparation Products And Raw materials |
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