Committed to preserving our shared environment – further details available on request.
Can be used in processes in compliance with cGMP standards.
Manufacture of consumables is accredited by the world renowned British Standards Institute.
Flexible supply chains, back up manufacturing and warehousing ensures supply risk reduction
Can be used in processes in compliance with GLP standards.
Products which are scaleable from lab or development to process scale.
Long to indefinite product shelf life, reduced process risk.
Supports pharma guidelines for reducing elemental impurities in APIs.
Further extractable information provided on request.
Raw materials certified free of materials of human or animal origin.
Chemical substances used in our manufacturing process do not require registration.
Able to withstand mechanical stirring and heating under normal reaction conditions.
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PS-Benzaldehyde is the resin-bound equivalent of benzaldehyde and is useful for scavenging various nucleophiles, including primary amines (selectively compared with secondary amines), hydrazines, also carbon-based nucleophiles such as Meldrum’s acid and organometallics.
The capacity of PS-Benzaldehyde is 1.2 mmol/g, based on phenylhydrazine uptake. Scavenging reactions typically use 3 equivalents of resin per equivalent of substrate to be scavenged. Various solvents can be used, including DCE, DCM, and DMF with a temperature range from 20 to 50 ˚C. PS-Benzaldehyde is stable at room temperature with no loss of activity observed over an extended period.
PS-Benzaldehyde resin (3 equivalents) in DCE was allowed to react with phenylhydrazine (1 equivalent) in the presence of a catalytic amount of glacial HOAc. The reaction was monitored by TLC and was complete after stirring for approximately 1 h at room temperature. The reaction may also be run without HOAc by heating for 1 h at 50˚C.
Scavenging Various Substrates
PS-Benzaldehyde (3 equivalents) was added to a solution of the substrate in DCE along with a catalyst if necessary. The mixture was stirred for the specified time and temperature, and the filtrate was analyzed by TLC for disappearance of the substrate by comparison with analytical standards.
Reductive Alkylation of Primary Amines
A THF solution (0.50 M) of N-(3-aminopropyl)morpholine (1.2 mL, 0.60 mmol) was added to a THF solution (0.50 M) of 1,4-cyclohexanedione mono-ethylene ketal (1.0 mL, 0.50 mmol). MP-Triacetoxyborohydride (2.0 mmol/g, 0.625 g, 1.25 mmol) was then added and the mixture was agitated for 16 h at room temperature. When the reaction was complete, PS-Benzaldehyde (0.42 g, 0.5 mmol) and THF (2 mL) were added and the mixture was further agitated for 6 h. The resin was filtered and washed with THF (2 x 4 mL). The combined solution was concentrated to afford the product secondary amine as the acetate salt in 77% yield and 100% purity. The secondary amine was characterized by gas chromatography and H NMR.