Hydrochloric Acid → HCID 22675472, compound

HRID 1106851Notes

Reaction equation

HRID 1106851 reaction equation
[CH2:1]([O:8][C:9]1[CH:31]=[CH:30][CH:29]=[CH:28][C:10]=1[CH2:11][C:12]([N:14]([C:17]1[CH:27]=[CH:26][C:20]([C:21]([O:23][CH2:24][CH3:25])=[O:22])=[CH:19][CH:18]=1)[CH2:15][CH3:16])=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl>C1COCC1>[CH2:1]([O:8][C:9]1[CH:31]=[CH:30][CH:29]=[CH:28][C:10]=1[CH2:11][CH2:12][N:14]([C:17]1[CH:18]=[CH:19][C:20]([C:21]([O:23][CH2:24][CH3:25])=[O:22])=[CH:26][CH:27]=1)[CH2:15][CH3:16])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

4

Procedure

Ethyl 4-[N-(2-benzyloxybenzylcarbonyl)-N-ethylamino]benzoate (8.1 g) was dissolved in THF (20 ml) and 1M borane tetrahydrofuran complex added. The reaction mixture was heated at reflux for 1 hour and cooled. 2N Hydrochloric acid (20 ml) was added. The volume of the reaction mixture was reduced to half the original by evaporation. Water (100 ml) was added and made basic (pH 8) by the addition of solid potassium carbonate and the mixture extracted with diethyl ether (3×30 ml). The combined extracts were dried over MgSO4 and evaporated. The residue was purified by MPLC, eluting with 1:1 dichloromethane/hexane, to give ethyl 4-[N-(2-(2-benzyloxyphenyl)ethyl)-N-ethylamino]benzoate (1.8 g) m.p. 76° C.

Workup

  1. addition1M borane tetrahydrofuran complex added
  2. temperatureThe reaction mixture was heated
  3. temperatureat reflux for 1 hour
  4. temperaturecooled
  5. customoriginal by evaporation
  6. additionWater (100 ml) was added
  7. additionby the addition of solid potassium carbonate
  8. extractionthe mixture extracted with diethyl ether (3×30 ml)
  9. dry with materialThe combined extracts were dried over MgSO4
  10. customevaporated
  11. customThe residue was purified by MPLC
  12. washeluting with 1:1 dichloromethane/hexane

Sources & evidence

ORD record
ord-e6076d3fa25641048e0d021c07a7c6a7
Source dataset
uspto-grants-2000_05
Patent number
US06057345

Reaction notes

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