1-Boc-beta-oxo-3-piperidinepropanoic acid methyl ester

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1-Boc-beta-oxo-3-piperidinepropanoic acid methyl ester Basic information
Product Name:1-Boc-beta-oxo-3-piperidinepropanoic acid methyl ester
Synonyms:tert-butyl 1-(2-hydroxypropyl)piperidin-4-ylcarbaMate;Methyl 1-Boc-b-oxo-3-piperidinepropanoate;3-Piperidinepropanoic acid, 1-[(1,1-dimethylethoxy)carbonyl]-β-oxo-, methyl ester;Methyl 3-(1-Boc-3-piperidyl)-3-oxopropanoate;tert-Butyl 3-(3-methoxy-3-oxopropanoyl)-piperidine-1-carboxylate - [B15156];N-Boc-3-(3-methoxy-3-oxopropanoyl)piperidine;1-Boc-beta-oxo-3-piperidinepropanoic acid methyl ester
CAS:891494-65-8
MF:C14H23NO5
MW:285.34
EINECS:
Product Categories:
Mol File:891494-65-8.mol
1-Boc-beta-oxo-3-piperidinepropanoic acid methyl ester Structure
1-Boc-beta-oxo-3-piperidinepropanoic acid methyl ester Chemical Properties
Boiling point 371.6±32.0 °C(Predicted)
density 1.130±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka10.37±0.20(Predicted)
Appearancepale yellow oil
Safety Information
MSDS Information
1-Boc-beta-oxo-3-piperidinepropanoic acid methyl ester Usage And Synthesis
Synthesis
Methanol

67-56-1

2,2-Dimethyl-1,3-dioxane-4,6-dione

2033-24-1

1-BOC-PIPERIDINE-3-CARBOXYLIC ACID

71381-75-4

1-BOC-BETA-OXO-3-PIPERIDINEPROPANOIC ACID METHYL ESTER

891494-65-8

Thionyl chloride (18.5 mL) was slowly added dropwise to a stirred mixture of 1-BOC-piperidine-3-carboxylic acid (50.0 g, 218 mmol) and pyridine (44.0 mL) in anhydrous dichloromethane (300 mL) under nitrogen protection. After the reaction mixture was stirred at 25 °C for 20 min, cyclic (sub)isopropyl malonate (35.0 g, 243 mmol) and 4-dimethylaminopyridine (66.6 g, 546 mmol) were added and stirring was continued for 1 h under nitrogen protection. Subsequently, ether (2 L) was added and the mixture was washed sequentially with 1 M hydrochloric acid (3 x 500 mL), saturated saline (500 mL), the organic layer was dried with anhydrous sodium sulfate, filtered and the solvent was concentrated. The residue was dissolved in methanol (580 mL) and reacted at reflux for 4 hours. After concentration to remove the solvent, the residue was purified by silica gel column chromatography with dichloromethane/ethyl acetate (10:1, v/v) as eluent. The final light yellow oily product N-Boc-3-(3-methoxy-3-oxopropionyl)piperidine (26.5 g, 43% yield) was obtained.

References[1] Patent: US2007/83044, 2007, A1. Location in patent: Page/Page column 32
[2] Patent: EP2069350, 2016, B1. Location in patent: Paragraph 0072; 0073
1-Boc-beta-oxo-3-piperidinepropanoic acid methyl ester Preparation Products And Raw materials
Raw materialsMethanol-->2,2-Dimethyl-1,3-dioxane-4,6-dione-->1-Boc-piperidine-3-carboxylic acid-->Pyridine-->Dichloromethane-->Thionyl chloride-->4-Dimethylaminopyridine
Preparation Productstert-butyl 3-(7-hydroxypyrazolo[1,5-a]pyrimidin-5-yl)piperidine-1-carboxylate
Tag:1-Boc-beta-oxo-3-piperidinepropanoic acid methyl ester(891494-65-8) Related Product Information
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