Identification | Back Directory | [Name]
1-N-Cbz-3-Methylpiperidine-3-carboxylic acid | [CAS]
174543-78-3 | [Synonyms]
1-N-Cbz-3-Methylpiperidine-3-carboxylic N-Cbz-3-Methylpiperidine-3-carboxylic acid 1-Cbz-3-methyl-3-piperidinecarboxylic acid 1-Cbz-3-Methylpiperidine-3-carboxylic Acid 1-N-Cbz-3-Methylpiperidine-3-carboxylic acid 1-Cbz-3-methyl-3-piperidinecarboxylic acid - [M13677] 1-[(benzyloxy)carbonyl]-3-methylpiperidine-3-carboxylic acid 3-Methyl-1,3-piperidinedicarboxylic acid 1-(phenylmethyl) ester 1,3-Piperidinedicarboxylic acid, 3-methyl-, 1-(phenylmethyl) ester | [Molecular Formula]
C15H19NO4 | [MDL Number]
MFCD11559118 | [MOL File]
174543-78-3.mol | [Molecular Weight]
277.32 |
Chemical Properties | Back Directory | [Boiling point ]
440.3±45.0 °C(Predicted) | [density ]
1.224 | [storage temp. ]
Store at room temperature | [pka]
4.52±0.20(Predicted) | [Appearance]
White to off-white Solid |
Hazard Information | Back Directory | [Synthesis]
Step C: 3-Benzyl 3-ethyl-3-methylpiperidine-1,3-dicarboxylate (3.0 g, 10.0 mmol) was dissolved in ethanol (15 mL) and aqueous LiOH solution (15.0 mL, 30.1 mmol) was added. The reaction mixture was stirred at 86 °C for 1 hour. After completion of the reaction, ethanol was removed by distillation under reduced pressure. Ether (30 mL) was added to the residue for extraction and the aqueous layer was separated. The aqueous layer was acidified to pH 3-4 with saturated potassium bisulfate solution and then extracted with ethyl acetate (50 mL). The organic layer was washed with brine and dried over anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure to give 1-(benzyloxycarbonyl)-3-methylpiperidine-3-carboxylic acid (2.6 g, 92% yield) as an oil. | [References]
[1] Patent: WO2009/140320, 2009, A1. Location in patent: Page/Page column 73 [2] Patent: US2006/149070, 2006, A1. Location in patent: Page/Page column 41 |
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NovoChemy Ltd.
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SynAsst Chemical.
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