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

HRID 993371
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 993371
[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]
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Komponenten

4

Edukt 2

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

Produkt 1

HCID 218769092-[4-(4-Isopropoxymethyl-benzyl)-phenyl]-imidazolineAusbeute 95,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3776IsopropanolLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

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 (3×20 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.

Aufarbeitung

  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 (3×20 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

Quellen und Nachweise

ORD-Eintrag
ord-8a3f85d3e208400c9b2fa6d632b8db3c
Quelldatensatz
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06472536B1

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