Hydrochloric Acid → 2-Isopropyl-5-methyl-cyclohexanecarboxylic acid (2-hydroxy-2-phenylethyl)-amide

HRID 18489

Reaktionsgleichung

Reaktionsgleichung von HRID 18489
CCN(C(C)C)C(C)C.[NH2:10][CH2:11][CH:12]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[OH:13].[CH:20]1([CH3:32])[CH2:25][CH2:24][CH:23]([CH:26]([CH3:28])[CH3:27])[CH:22]([C:29](Cl)=[O:30])[CH2:21]1.Cl>C(Cl)Cl>[OH:13][CH:12]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[CH2:11][NH:10][C:29]([CH:22]1[CH2:21][CH:20]([CH3:32])[CH2:25][CH2:24][CH:23]1[CH:26]([CH3:28])[CH3:27])=[O:30]

Komponenten

6

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

A 500 mL round bottom flask equipped with stir bar was charged with CH2Cl2 (200 mL), DIEA (28 g, 0.219 mol), and 2-Amino-1-phenyl-ethanol (10 g, 0.073 mol) and cooled to 0° C. Menthoyl chloride (14.8 g, 0.073 mol) was added drop wise over a 15 min period. Once the addition was complete the reaction was allowed to warm to ambient temperature and stirred 2 h. CH2Cl2 (100 mL) and 1N HCl (100 mL) was added to the reaction mixture and stirred for an additional 20 min. The heterogeneous mixture was transferred to a separatory funnel where the aqueous phase was separated and re-extracted with CH2Cl2 (2×100 mL). The organic phases were combined and washed with 1N HCl (8×100 mL), H2O (1×100 mL), 1N NaOH (2×100 mL), brine (100 mL), dried over MgSO4, filtered and concentrated under reduced pressure. The residue was eluted through a plug of silica gel (50% ethyl acetate/hexane for elution) provided the title compounds as colorless solid (18.8 g, 85%).

Aufarbeitung

  1. customA 500 mL round bottom flask equipped
  2. additionOnce the addition
  3. temperatureto warm to ambient temperature
  4. stirringstirred 2 h
  5. stirringstirred for an additional 20 min
  6. customThe heterogeneous mixture was transferred to a separatory funnel
  7. customwhere the aqueous phase was separated
  8. extractionre-extracted with CH2Cl2 (2×100 mL)
  9. washwashed with 1N HCl (8×100 mL), H2O (1×100 mL), 1N NaOH (2×100 mL), brine (100 mL)
  10. dry with materialdried over MgSO4
  11. filtrationfiltered
  12. concentrationconcentrated under reduced pressure
  13. washThe residue was eluted through a plug of silica gel (50% ethyl acetate/hexane for elution)

Quellen und Nachweise

ORD-Eintrag
ord-0dc6aaddce7549f4b2a1379ba3230698
Quelldatensatz
uspto-grants-2010_06
Patentnummer
US07741355B2

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