Hydrochloric Acid → 3-(4-Bromophenyl)-N-methylpropan-1-amine

Temperature

0 °C

Borane in THF (1.0 M, 28 mL, 28 mmol) was added dropwise to a solution of 22A (1.6 g, 7.0 mmol) in THF (17.5 mL). After stirring the reaction mixture for 30 min at 0° C. the mixture was refluxed for 4 h. Methanol (20 mL) was added to the mixture at 0° C. followed by the addition of 20 mL 6.0 M HCl dropwise. After refluxing for 30 min the volatiles were removed in vacuo. 50% NaOH (12 mL) was added dropwise while maintaining the temperature below 30° C. The resulting mixture was diluted with water (100 mL) and extracted with diethyl ether (3×100 mL). The organics were combined, washed with brine, dried over Na2SO4 and concentrated in vacuo to yield 22B (1.57 g, 97%) as a clear oil. MS (ESI) m/z 227.99/229.99 (M+H)+.

1. temperaturewas refluxed for 4 h
2. temperatureAfter refluxing for 30 min the volatiles
3. customwere removed in vacuo
4. addition50% NaOH (12 mL) was added dropwise
5. temperaturewhile maintaining the temperature below 30° C
6. additionThe resulting mixture was diluted with water (100 mL)
7. extractionextracted with diethyl ether (3×100 mL)
8. washwashed with brine
9. dry with materialdried over Na2SO4
10. concentrationconcentrated in vacuo

ORD record

ord-11fef40bfd3a47f9af374794c0fb99df

Source dataset

uspto-grants-2009_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07592331B2