- 1-Boc-3-Formylpiperidine
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- $200.00 / 1KG
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2023-06-26
- CAS:118156-93-7
- Min. Order: 10g
- Purity: 99%
- Supply Ability: 500kg/month
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| | 1-BOC-3-PIPERIDINECARBOXALDEHYDE Basic information |
| Product Name: | 1-BOC-3-PIPERIDINECARBOXALDEHYDE | | Synonyms: | N-BOC-3-PIPERIDINYLCARBOXALDEHYDE;N-BOC-3-FORMYLPIPERIDINE;BOC-3-PIPERIDINECARBOXALDEHYDE;BUTTPARK 147\06-01;1-BOC-3-PIPERIDINECARBOXALDEHYDE;1-N-BOC-3-FORMYLPIPERIDINE;3-FORMYLPIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER;1-Piperidinecarboxylic acid, 3-formyl-, 1,1-dimethylethyl ester | | CAS: | 118156-93-7 | | MF: | C11H19NO3 | | MW: | 213.27 | | EINECS: | | | Product Categories: | pharmacetical;Piperidine | | Mol File: | 118156-93-7.mol |  |
| | 1-BOC-3-PIPERIDINECARBOXALDEHYDE Chemical Properties |
| Boiling point | 295.4±33.0 °C(Predicted) | | density | 1.114±0.06 g/cm3(Predicted) | | storage temp. | Inert atmosphere,Store in freezer, under -20°C | | form | liquid | | pka | -2.29±0.40(Predicted) | | color | Clear, light yellow | | Sensitive | Air Sensitive | | InChI | InChI=1S/C11H19NO3/c1-11(2,3)15-10(14)12-6-4-5-9(7-12)8-13/h8-9H,4-7H2,1-3H3 | | InChIKey | CTVHINDANRPFIL-UHFFFAOYSA-N | | SMILES | N1(C(OC(C)(C)C)=O)CCCC(C=O)C1 | | CAS DataBase Reference | 118156-93-7(CAS DataBase Reference) |
| | 1-BOC-3-PIPERIDINECARBOXALDEHYDE Usage And Synthesis |
| Chemical Properties | Colorless liquid | | Uses | 1-Boc-piperidine-3-carboxaldehyde is used as an organic chemical synthesis intermediate. | | Synthesis | General procedure for the synthesis of 1-Boc-3-piperidinecarboxaldehyde from tert-butyl 3-(hydroxymethyl)piperidine-1-carboxylate: a solution of dimethylsulfoxide (DMSO, 0.18 mL, 2.6 mmol) in dichloromethane (CH2Cl2, 5 mL) was slowly added dropwise at -78 °C to a solution of oxalyl chloride (2 M in CH2Cl2, 0.65 mL, 1.3 mmol ) in a solution of methylene chloride (4 mL). The reaction mixture was stirred at -68 °C for 15 min. Subsequently, tert-butyl 3-(hydroxymethyl)piperidine-1-carboxylate (0.22 g, 1.0 mmol) was added dropwise to a dichloromethane (4 mL) solution. After continued stirring at -78 °C for 15 min, triethylamine (Et3N, 6 mL) was added. The reaction mixture was warmed to room temperature and stirred for 16 hours. Upon completion of the reaction, water was added to quench the reaction and the mixture was extracted with ether. The organic layers were combined, dried over anhydrous sodium sulfate (Na2SO4) and concentrated under reduced pressure to give the yellow oily product 1-Boc-3-piperidinecarboxaldehyde (0.20 g, 92% yield). The crude product could be directly used in the subsequent reaction without further purification. Mass spectrum (ESI) m/z 214 (M + 1). | | References | [1] Patent: WO2006/62465, 2006, A1. Location in patent: Page/Page column 40
[2] Patent: US2004/229864, 2004, A1. Location in patent: Page/Page column 11
[3] Patent: US2017/313683, 2017, A1. Location in patent: Paragraph 0560-0561
[4] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 4, p. 1368 - 1373
[5] Patent: US2014/31354, 2014, A1. Location in patent: Paragraph 0421; 0422 |
| | 1-BOC-3-PIPERIDINECARBOXALDEHYDE Preparation Products And Raw materials |
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