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2-Chloroimidazoline sulfate → 2-[4-(4-Isopropoxymethyl-benzyl)-phenyl]-imidazoline

HRID 634795
Notes
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Reaction equation

HRID 634795 reaction equation
[CH:1]([O:4][CH2:5][C:6]1[CH:19]=[CH:18][C:9]([CH2:10][C:11]2[CH:16]=[CH:15][C:14](N)=[CH:13][CH:12]=2)=[CH:8][CH:7]=1)([CH3:3])[CH3:2].S(O)(O)(=O)=O.Cl[C:26]1[NH:27][CH2:28][CH2:29][N:30]=1>C(O)(C)C>[CH:1]([O:4][CH2:5][C:6]1[CH:19]=[CH:18][C:9]([CH2:10][C:11]2[CH:16]=[CH:15][C:14]([C:26]3[NH:30][CH2:29][CH2:28][N:27]=3)=[CH:13][CH:12]=2)=[CH:8][CH:7]=1)([CH3:3])[CH3:2]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 125033982-Chloroimidazoline sulfateHCID 218768564-(4-Isopropoxymethylbenzyl)-phenylamine

Product 1

HCID 218769092-[4-(4-Isopropoxymethyl-benzyl)-phenyl]-imidazolineYield 95.6%

Reagents, catalysts & solvents 1

HCID 3776IsopropanolSolvent

Conditions

Temperature
80 °C

Procedure

To a solution of 4-(4-isopropoxymethylbenzyl)-phenylamine (400 mg, 1.57 mmol) in isopropanol (4.8 mL) at 20° C. under argon atmosphere was added 2-chloro-2-imidazoline sulfate (382 mg, 1.88 mmol). The mixture was heated to 80° C. and stirred for 3 hours. The solvent was evaporated in vacuo, and water and 10% sodium hydroxide was added to pH 11-12. The basic aqueous phase was extracted with dichloromethane (3x 20 mL), and the combined organic layers were washed with water, dried (Na2SO4), and evaporated in vacuo. The crude product was purified by flash chromatography, washed with 0.07M potassium carbonate, and concentrated to give pure 2-[4-(4-isopropoxymethyl-benzyl)-phenyl]-imidazoline (463 mg, 91%) as a clear oil.

Workup

  1. customThe solvent was evaporated in vacuo, and water and 10% sodium hydroxide
  2. additionwas added to pH 11-12
  3. extractionThe basic aqueous phase was extracted with dichloromethane (3x 20 mL)
  4. washthe combined organic layers were washed with water
  5. dry with materialdried (Na2SO4)
  6. customevaporated in vacuo
  7. customThe crude product was purified by flash chromatography
  8. washwashed with 0.07M potassium carbonate
  9. concentrationconcentrated

Sources & evidence

ORD record
ord-8b19a98a856c46679d05d8cc0ce8aeb3
Source dataset
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06184242B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes