Methylamine → Benzenemethanamine, 4-bromo-N-methyl-

800 ml of an 8% solution of methylamine in toluene are added, whilst cooling with ice, to 100 g of 4-bromobenzaldehyde and 300 g of molecular sieve (3 Angstroms). The mixture is stirred overnight at ambient temperature, suction filtered to remove the molecular sieve and the solvent is evaporated off. The residue is dissolved in 1.4 litres of ice cold methanol and 48 g of sodium borohydride are added in batches whilst cooling with ice. Then the mixture is stirred for 30 minutes at 0° C., for one hour at 10° C. and for two hours at ambient temperature, then evaporated to dryness, the residue is taken up in ice water, acidified with half concentrated hydrochloric acid and extracted twice with ether. The ether is discarded, the aqueous phase is made alkaline with concentrated sodium hydroxide solution whilst cooling and then extracted three times with ether. The organic phase is washed with water and saturated saline solution, dried and evaporated down. 96.8 g of N-methyl-4-bromobenzylamine are obtained in the form of a colourless oil.

1. filtrationsuction filtered
2. customto remove the molecular sieve
3. customthe solvent is evaporated off
4. dissolutionThe residue is dissolved in 1.4 litres of ice cold methanol
5. addition48 g of sodium borohydride are added in batches
6. temperaturewhilst cooling with ice
7. stirringThen the mixture is stirred for 30 minutes at 0° C., for one hour at 10° C. and for two hours at ambient temperature
8. customevaporated to dryness
9. extractionextracted twice with ether
10. temperaturewhilst cooling
11. extractionextracted three times with ether
12. washThe organic phase is washed with water and saturated saline solution
13. customdried
14. customevaporated down

ORD record

ord-580d54b5d5064182a56c0c28fc21221f

Source dataset

uspto-grants-1995_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05455273