Hydrochloric Acid → 2-{[2-(2-Chlorophenyl)ethyl](methyl)amino}ethan-1-ol

HRID 2413109Notes

Reaction equation

HRID 2413109 reaction equation
B.[Cl:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:9][C:10]([N:12]([CH2:14][CH2:15][OH:16])[CH3:13])=O.Cl>O1CCCC1>[Cl:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:9][CH2:10][N:12]([CH3:13])[CH2:14][CH2:15][OH:16]

Participants

5

Procedure

To 400 ml. of a 1 mol solution of borane in tetrahydrofuran was added dropwise a solution of 43 g. of the above amide in 350 ml. of tetrahydrofuran at a rate sufficient to maintain a gentle reflux. After addition was complete, the solution was refluxed for two hours, cooled in an ice bath and treated carefully with dilute hydrochloric acid to destroy excess borane. The majority of the solvent was removed under vacuum and the residue heated on a steam bath for one hour. The mixture was diluted with 300 ml. of water and extracted with ether. The aqueous layer was made basic with 40% sodium hydroxide and extracted with ether. The combined basic extracts were washed with water and saturated sodium chloride, dried and evaporated to give 2-[[2-(2-chlorophenyl)-ethyl]-methylamino]ethanol.

Workup

  1. additionAfter addition
  2. temperaturethe solution was refluxed for two hours
  3. temperaturecooled in an ice bath
  4. customto destroy excess borane
  5. customThe majority of the solvent was removed under vacuum
  6. temperaturethe residue heated on a steam bath for one hour
  7. additionThe mixture was diluted with 300 ml
  8. extractionof water and extracted with ether
  9. extractionextracted with ether
  10. washThe combined basic extracts were washed with water and saturated sodium chloride
  11. customdried
  12. customevaporated

Sources & evidence

ORD record
ord-8c0af4f70b2d42a5862a4a519edbc68e
Source dataset
uspto-grants-1985_01
Patent number
US04496558

Reaction notes

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