Benzyl 4-bromotetrahydro-1(2H)-pyridinecarboxylate

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Benzyl 4-bromotetrahydro-1(2H)-pyridinecarboxylate Basic information
Product Name:Benzyl 4-bromotetrahydro-1(2H)-pyridinecarboxylate
Synonyms:N-CBZ-4-BROMO-PIPERIDINE;4-Bromo-N-Cbz-piperidine, Benzyl 4-bromopiperidine-1-carboxylate;4-Bromopiperidine-1-carboxylic acid benzyl ester;BUTTPARK 93\50-52;4-Bromopiperidine, N-CBZ protected;4-BROMO-N-Z-PIPERIDINE,96%;4-bromo-n-cbz piperidine;Benzyl 4-bromotetrahydro-1(2H)-pyridinecarboxylate, 90+%
CAS:166953-64-6
MF:C13H16BrNO2
MW:298.18
EINECS:
Product Categories:C12 to C13;Building Blocks;C13;API intermediates;Chemical Synthesis;Halogenated Heterocycles;Heterocyclic Building Blocks;Piperidines
Mol File:166953-64-6.mol
Benzyl 4-bromotetrahydro-1(2H)-pyridinecarboxylate Structure
Benzyl 4-bromotetrahydro-1(2H)-pyridinecarboxylate Chemical Properties
Boiling point 144 °C
density 1.374 g/mL at 25 °C(lit.)
refractive index n20/D 1.5590(lit.)
Fp >230 °F
storage temp. Inert atmosphere,Room Temperature
pka-2.82±0.40(Predicted)
AppearanceColorless to light yellow Liquid
InChI1S/C13H16BrNO2/c14-12-6-8-15(9-7-12)13(16)17-10-11-4-2-1-3-5-11/h1-5,12H,6-10H2
InChIKeyBFWKSPOSMPKTSV-UHFFFAOYSA-N
SMILESBrC1CCN(CC1)C(=O)OCc2ccccc2
Safety Information
Hazard Codes Xi
WGK Germany 3
Hazard Note Irritant
HS Code 29333999
Storage Class10 - Combustible liquids
MSDS Information
ProviderLanguage
SigmaAldrich English
Benzyl 4-bromotetrahydro-1(2H)-pyridinecarboxylate Usage And Synthesis
Synthesis
4-BROMO-PIPERIDINE

90633-18-4

Benzyl chloroformate

501-53-1

BENZYL 4-BROMOTETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE

166953-64-6

To a reaction flask was added 4-bromopiperidine hydrobromide (5.0 g, 20.4 mmol) and dichloromethane (80 mL) followed by saturated sodium bicarbonate solution (160 mL) and benzyl chloroformate (3.7 mL, 24.5 mmol). The reaction mixture was stirred at 23 °C for 22 hours. Upon completion of the reaction, the mixture was transferred to a partition funnel and the product was extracted with dichloromethane. The organic phases were combined, washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated. Purification by silica gel column chromatography (eluent: hexane/ethyl acetate = 8:1) afforded benzyl 4-bromopiperidine-1-carboxylate (3.02 g, 10.1 mmol, 50% yield) as a colorless oil. Mass spectrum (MS): m/e 298.

References[1] Patent: WO2003/103669, 2003, A1. Location in patent: Page 44-45
Tag:Benzyl 4-bromotetrahydro-1(2H)-pyridinecarboxylate(166953-64-6) Related Product Information
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