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| | 1-BOC-4-(4-BROMO-BENZOYL)-PIPERIDINE Basic information |
| Product Name: | 1-BOC-4-(4-BROMO-BENZOYL)-PIPERIDINE | | Synonyms: | 1-BOC-4-(4-BROMO-BENZOYL)-PIPERIDINE;tert-butyl 4-(4-broMobenzoyl)piperidine-1-carboxylate;tert-butyl 4-[(4-broMophenyl)carbonyl]piperidine-1-carboxylate;1-Piperidinecarboxylic acid, 4-(4-bromobenzoyl)-, 1,1-dimethylethyl ester;4-(4-bromobenzoyl)piperidine-1-carboxylic acid tert-butyl ester | | CAS: | 439811-37-7 | | MF: | C17H22BrNO3 | | MW: | 368.27 | | EINECS: | 200-589-5 | | Product Categories: | | | Mol File: | 439811-37-7.mol |  |
| | 1-BOC-4-(4-BROMO-BENZOYL)-PIPERIDINE Chemical Properties |
| Boiling point | 452.3±40.0 °C(Predicted) | | density | 1.325±0.06 g/cm3(Predicted) | | storage temp. | 2-8°C | | pka | -2.47±0.40(Predicted) | | Appearance | Off-white to light yellow Solid |
| | 1-BOC-4-(4-BROMO-BENZOYL)-PIPERIDINE Usage And Synthesis |
| Synthesis | Step 1. Synthesis of tert-butyl 4-(4-bromobenzoyl)-piperidine-1-carboxylate. To a 250 mL round bottom flask was added 4-(4-bromobenzoyl)piperidine (5 g, 20 mmol), tetrahydrofuran (30 mL), water (30 mL), sodium carbonate (10 g, 90 mmol) and di-tert-butyl dicarbonate (4.35 g, 20.0 mmol). The reaction mixture was stirred at room temperature for 2 h and then partitioned with ethyl acetate and water. The aqueous layer was extracted twice with ethyl acetate, the organic phases were combined, washed with brine, dried, filtered and concentrated to give 7.1 g (100% yield) of tert-butyl 4-(4-bromobenzoyl)-piperidine-1-carboxylate. | | References | [1] Patent: WO2016/205590, 2016, A1. Location in patent: Paragraph 00596
[2] Patent: WO2013/147711, 2013, A1. Location in patent: Page/Page column 231
[3] Patent: US2014/371199, 2014, A1. Location in patent: Paragraph 0801
[4] Patent: US2005/54628, 2005, A1. Location in patent: Page/Page column 23-24
[5] Patent: US2005/49269, 2005, A1. Location in patent: Page/Page column 12; 21 |
| | 1-BOC-4-(4-BROMO-BENZOYL)-PIPERIDINE Preparation Products And Raw materials |
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