Hydrochloric Acid → N-(4-fluorobenzyl)ethanamine

N-(4-Fluorobenzyl)acetamide (1.344 g, 8.039 mmol) was dissolved in THF (100 ml) and was cooled to zero degrees under argon atmosphere. (Methylthio)methene compound with borane (1:1) (1.527 g, 20.098 mmol) was added and the mixture was refluxed overnight at RT. HCl (15 ml, 10%) was gently added and was stirred overnight. The solvent was removed by evaporation. Diethyl ether (20 ml) was added and the product was extracted to the water phase by K2CO3 (3×15 ml). The water phase was acidified by HCl (10 ml, 10%) and the product was extracted to the organic phase by EtOAc (3×15 ml). The organic phase was dried (MgSO4) and the solvent was removed by evaporation to give 0.309 g of N-(4-fluorobenzyl)ethanamine (yield 25.1%).

1. temperaturewas cooled to zero degrees under argon atmosphere
2. customThe solvent was removed by evaporation
3. additionDiethyl ether (20 ml) was added
4. extractionthe product was extracted to the water phase by K2CO3 (3×15 ml)
5. extractionthe product was extracted to the organic phase by EtOAc (3×15 ml)
6. dry with materialThe organic phase was dried (MgSO4)
7. customthe solvent was removed by evaporation

ORD record

ord-53e5602107754c2e8405dd1be097fb73

Source dataset

uspto-grants-2008_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07351858B2