Methyl N-Boc-4-hydroxypiperidine-3-carboxylate

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Methyl N-Boc-4-hydroxypiperidine-3-carboxylate manufacturers

Methyl N-Boc-4-hydroxypiperidine-3-carboxylate Basic information
Product Name:Methyl N-Boc-4-hydroxypiperidine-3-carboxylate
Synonyms:Methyl N-Boc-4-hydroxypiperidine-3-carboxylate;1-tert-butyl 3-Methyl 4-hydroxypiperidine-1,3-dicarboxylate;4-Hydroxy-1,3-piperidinedicarboxylic acid 1-(1,1-dimethylethyl) 3-methyl ester;Methyl N-(tert-Butoxycarbonyl)-4-hydroxypiperidine-3-carboxylate;1-tert-Butyl 3-Methyl 4-hydroxy-1,3-piperidinedicarboxylate;1,3-Piperidinedicarboxylic acid, 4-hydroxy-, 1-(1,1-diMethylethyl) 3-Methyl ester;Methyl N-Boc-4-hydroxypiperidine-3-;N-Boc-4-hydroxypiperidine-3-carboxylate
CAS:406212-51-9
MF:C12H21NO5
MW:259.3
EINECS:
Product Categories:
Mol File:406212-51-9.mol
Methyl N-Boc-4-hydroxypiperidine-3-carboxylate Structure
Methyl N-Boc-4-hydroxypiperidine-3-carboxylate Chemical Properties
Boiling point 352.1±42.0 °C(Predicted)
density 1.182±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka14.12±0.40(Predicted)
Safety Information
MSDS Information
Methyl N-Boc-4-hydroxypiperidine-3-carboxylate Usage And Synthesis
Synthesis
1-tert-Butyl 3-methyl 4-oxopiperidine-1,3-dicarboxylate

161491-24-3

Methyl N-Boc-4-hydroxypiperidine-3-carboxylate

406212-51-9

General procedure for the synthesis of methyl N-Boc-4-hydroxypiperidine-3-carboxylate from tert-butyl 4-oxopiperidine-1-carboxylate-3-carboxylate: To a solution of tert-butyl 1-(1,3-piperidinedicarboxylate) in methanol (800 mL) of 3-oxo-1,3-piperidinedicarboxylic acid (134.0 g, 520.8 mmol) was added in batches at 0 °C NaBH4 (9.85 g, 260.4 mmol). The reaction mixture was stirred overnight and allowed to warm up naturally to room temperature. After completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was dissolved in ethyl acetate, washed with saturated brine, dried over anhydrous MgSO4, filtered and concentrated under reduced pressure to afford 3-tert-butyl 3-methyl-4-hydroxy-1,3-piperidinedicarboxylate (120.8 g, 90% yield), which could be used for the next reaction without further purification.

References[1] Patent: US6562811, 2003, B1
Methyl N-Boc-4-hydroxypiperidine-3-carboxylate Preparation Products And Raw materials
Raw materials1-tert-Butyl 3-methyl 4-oxopiperidine-1,3-dicarboxylate-->Methanol-->Ethyl acetate-->Sodium borohydride
Tag:Methyl N-Boc-4-hydroxypiperidine-3-carboxylate(406212-51-9) Related Product Information
4-HYDROXY-PIPERIDINE-3-CARBOXYLIC ACID METHYL ESTER Methyl 6-bromo-3-oxo-3,4-dihydropyrazine-2-carboxylate 1-(tert-butoxycarbonyl)-4-hydroxypiperidine-3-carboxylic acid 1-tert-Butyl 3-methyl 4-oxopiperidine-1,3-dicarboxylate 4-HYDROXY-PIPERIDINE-1,3-DICARBOXYLIC ACID 1-TERT-BUTYL ESTER Methyl 4-hydroxypiperidine-3-carboxylate hydrochloride