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141047-46-3

4-HYDROXY-PIPERIDINE-1-CARBALDEHYDE synthesis

5synthesis methods
201230-82-2 Synthesis
carbon monoxide

201230-82-2
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4-HYDROXY-PIPERIDINE-1-CARBALDEHYDE

141047-46-3
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Yield:141047-46-3 97%

Reaction Conditions:

with water-soluble Na+ in red mud in methanol at 130; under 15001.5 Torr;Autoclave;Green chemistry;

Steps:

2.3. General procedure for the carbonylation of amines to N-formamides

General procedure: In a typical reaction, the 2 mg of WSS or 50 mg of red mud catalyst isweighed into a 10 mL reactor containing a stir bar. The requiredamounts of morpholine (0.5 mmol), methanol (2 mL) is added. At roomtemperature, the batch reactor is charged with 2.0 MPa of CO. Themixture is stirred at 130 C for 12 h. Afterwards, the autoclave is cooledto room temperature and the pressure is carefully released. The productsof the reaction are analyzed by gas chromatography (GC, Agilent 7890A)and GC-MS spectrometry (MS, Shimadzu). Chromatography purificationsare carried out over diatomite with ethyl acetate as eluent.Analytical data of literature-reported compounds are in accord withreported data. 1H, 13C NMR spectra are recorded on AVANCE NEO400MHZ NMR spectrometer (Bruker). Carbonylation of other amines toN-formamides is carried out with similar procedure.

References:

Chen, Dilong;Ding, Yuxiao;Xia, Chungu;He, Lin;Cao, Yanwei [Molecular catalysis,2022,vol. 533,art. no. 112761]

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