Hydrochloric Acid → 830348-34-0

HRID 1518593Notes

Reaction equation

HRID 1518593 reaction equation
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][C:9]#[N:10])=[N:6][CH:7]=1.B.O1CCCC1.Cl.O>C1COCC1>[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][CH2:9][NH2:10])=[N:6][CH:7]=1

Participants

6

Conditions

Temperature
60 °C

Procedure

To a solution of 18 g of crude 2-(5-methylpyridin-2-yl)acetonitrile in dry THF (100 mL) was added dropwise Borane-tetrahydrofuran complex (1.0 M in THF, 232 mL, 232.5 mmol, 4 eq) at 0° C. under N2 atmosphere. The reaction mixture was then heated to 60° C. overnight. The reaction was cooled to room temperature, aq.HCl (6 N, 40 mL) was added carefully and the reaction mixture was then heated at 70° C. for 2 hrs. After cooling, water was added and the resulting solution was washed with ether. The aqueous layer was basified with aq. NaOH (10 N) at 0° C. and saturated with K2CO3 then extracted with ether (5×100 mL). The organic layer was dried over MgSO4, filtered and evaporated to give 7.6 g of crude 2-(5-methylpyridin-2-yl)ethanamine. (96% crude yield)

Workup

  1. temperatureThe reaction was cooled to room temperature
  2. temperaturethe reaction mixture was then heated at 70° C. for 2 hrs
  3. temperatureAfter cooling
  4. washthe resulting solution was washed with ether
  5. customwas basified with aq. NaOH (10 N) at 0° C. and saturated with K2CO3
  6. extractionthen extracted with ether (5×100 mL)
  7. dry with materialThe organic layer was dried over MgSO4
  8. filtrationfiltered
  9. customevaporated

Sources & evidence

ORD record
ord-4184a2ab89c04c4d956d997123143e0a
Source dataset
uspto-grants-2015_07
Patent number
US09072313B2

Reaction notes

Loading…