1-Boc-4-formyl-4-methyl-piperidine

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Company Name: Energy Chemical  Gold
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Company Name: Changzhou Shili Pharmaceutical Technology Co., Ltd  Gold
Tel: 051988727299; 13961229012
Email: shitech@163.com
Company Name: Pure Chemistry Scientific Inc.  
Tel: 001-857-928-2050 or 1-888-588-9418
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Company Name: Shanghai AmasPharm Co., Ltd.  
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Company Name: Shanghai Sunway Pharmaceutical Technology Co., Ltd  
Tel: 13761987713
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1-Boc-4-formyl-4-methyl-piperidine manufacturers

1-Boc-4-formyl-4-methyl-piperidine Basic information
Product Name:1-Boc-4-formyl-4-methyl-piperidine
Synonyms:2-Methyl-2-Propanyl 4-ForMyl-4-Methyl-1-Piperidinecarboxylate;1-tert-Butoxycarbonyl-4-methylpiperidine-4-carboxaldehyde;4-Formyl-4-methylpiperidine-1-carboxylic acid;N-tert-Butoxycarbonyl-4-methyl-4-piperidine carboxaldehyde;1-Piperidinecarboxylic acid, 4-formyl-4-methyl-, 1,1-dimethylethyl ester;TERT-BUTYL 4-FORMYL-4-METHYLPIPERIDINE-1-CARBOXYLAT;1-Boc-4-methylpiperidine-4-carbaldehyde;tert-Butyl 4-formyl-4-methylpiperidine-1-carboxylate
CAS:189442-92-0
MF:C12H21NO3
MW:227.3
EINECS:
Product Categories:
Mol File:189442-92-0.mol
1-Boc-4-formyl-4-methyl-piperidine Structure
1-Boc-4-formyl-4-methyl-piperidine Chemical Properties
Boiling point 300.3±35.0 °C(Predicted)
density 1.083±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Store in freezer, under -20°C
pka-2.10±0.40(Predicted)
AppearanceColorless to light yellow Liquid
Safety Information
MSDS Information
1-Boc-4-formyl-4-methyl-piperidine Usage And Synthesis
Synthesis
1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde

137076-22-3

Iodomethane

74-88-4

1-BOC-4-FORMYL-4-METHYL-PIPERIDINE

189442-92-0

1-Boc piperidine-4-carbaldehyde (35.0 g, 164.1 mmol) was dissolved in dichloromethane (200 mL) and the solution was cooled to 0 °C. Potassium tert-butoxide (23.9 g, 213 mmol) was added to the solution with stirring, followed by slow addition of iodomethane (69.9 g, 492 mmol). The reaction mixture was stirred at 0 °C for 30 min, then gradually warmed to room temperature and continued stirring for 1.5 h. The reaction was completed by pouring the mixture into the solution. After completion of the reaction, the mixture was poured into brine (400 mL) and the organic layer was separated. The organic layer was dried with anhydrous sodium sulfate, filtered and concentrated. The crude product was purified by silica gel column chromatography to afford 1-Boc-4-formyl-4-methylpiperidine (16.36 g, 72.0 mmol, 43.8% yield).

References[1] Patent: WO2008/118718, 2008, A2. Location in patent: Page/Page column 84
[2] Patent: WO2014/28384, 2014, A1. Location in patent: Page/Page column 112
[3] Patent: WO2014/164467, 2014, A1. Location in patent: Page/Page column 65
[4] Patent: WO2014/164428, 2014, A1. Location in patent: Page/Page column 61
[5] Patent: WO2013/127828, 2013, A1. Location in patent: Page/Page column 62
1-Boc-4-formyl-4-methyl-piperidine Preparation Products And Raw materials
Raw materials1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde-->Iodomethane-->Dichloromethane-->Potassium-->Recombinant Human Telomerase
Tag:1-Boc-4-formyl-4-methyl-piperidine(189442-92-0) Related Product Information
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