ChemicalBook--->CAS DataBase List--->406212-51-9

406212-51-9

406212-51-9 Structure

406212-51-9 Structure
IdentificationBack Directory
[Name]

Methyl N-Boc-4-hydroxypiperidine-3-carboxylate
[CAS]

406212-51-9
[Synonyms]

Methyl N-Boc-4-hydroxypiperidine-3-carboxylate
1-tert-butyl 3-Methyl 4-hydroxypiperidine-1,3-dicarboxylate
1-tert-Butyl 3-Methyl 4-hydroxy-1,3-piperidinedicarboxylate
Methyl N-(tert-Butoxycarbonyl)-4-hydroxypiperidine-3-carboxylate
4-Hydroxy-1,3-piperidinedicarboxylic acid 1-(1,1-dimethylethyl) 3-methyl ester
1,3-Piperidinedicarboxylic acid, 4-hydroxy-, 1-(1,1-diMethylethyl) 3-Methyl ester
[Molecular Formula]

C12H21NO5
[MDL Number]

MFCD18651699
[MOL File]

406212-51-9.mol
[Molecular Weight]

259.3
Chemical PropertiesBack Directory
[Boiling point ]

352.1±42.0 °C(Predicted)
[density ]

1.182±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

14.12±0.40(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[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
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