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Hydrochloric Acid → 4-Methoxymethyl-pyrrolidine-1,2-dicarboxylic acid 2-[2-(4-bromo-phenyl)-2-oxo-ethyl]ester 1-tert-butyl ester

HRID 71984
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 71984
[CH3:1][O:2][C:3]([CH:5]1[CH2:9][CH:8]([CH2:10][O:11][CH3:12])[CH2:7][N:6]1[C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])=[O:4].[Li+].[OH-].Cl.BrC[C:25]([C:27]1[CH:32]=[CH:31][C:30]([Br:33])=[CH:29][CH:28]=1)=[O:26].C(N(CC)CC)C>CO>[C:16]([O:15][C:13]([N:6]1[CH2:7][CH:8]([CH2:10][O:11][CH3:12])[CH2:9][CH:5]1[C:3]([O:2][CH2:1][C:25]([C:27]1[CH:32]=[CH:31][C:30]([Br:33])=[CH:29][CH:28]=1)=[O:26])=[O:4])=[O:14])([CH3:19])([CH3:18])[CH3:17]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 5

HCID 313Hydrochloric AcidHCID 3939Lithium HydroxideHCID 74544-Bromophenacyl bromideHCID 8471TriethylamineHCID 66621318O1-tert-butyl O2-methyl 4-(methoxymethyl)pyrrolidine-1,2-dicarboxylate

Produkt 1

HCID 66620783
4-Methoxymethyl-pyrrolidine-1,2-dicarboxylic acid 2-[2-(4-bromo-phenyl)-2-oxo-ethyl]ester 1-tert-butyl ester
Ausbeute 97,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

4-Methoxymethyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester (461 mg, 1.68 mmol) was dissolved in MeOH (17 mL) and LiOH (1 M in H2O, 8.5 mL, 8.5 mmol) was added. After stirring at RT for 5 h, the MeOH was removed under reduced pressure. The aqueous solution was poured into a separatory funnel, diluted with 1 M HCl (9 mL, 9 mmol) and extracted with DCM (3×). The combined organics were dried over MgSO4, filtered and concentrated. The residue was dissolved in MeCN (17 mL) and treated with 2,4′-dibromoacetophenone (514 mg, 1.85 mmol), and triethylamine (0.258 mL, 1.85 mmol). After stirring for 2 h, the solvent was removed and the solid was suspended in EtOAc. The organic layer was washed with saturated aqueous NaHCO3 and brine then dried over MgSO4, filtered and concentrated. The crude residue was purified by silica column chromatography (15% to 35% EtOAc/Hex) to afford the title compound (746 mg, 97%).

Aufarbeitung

  1. customthe MeOH was removed under reduced pressure
  2. additionThe aqueous solution was poured into a separatory funnel
  3. extractionextracted with DCM (3×)
  4. dry with materialThe combined organics were dried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. dissolutionThe residue was dissolved in MeCN (17 mL)
  8. stirringAfter stirring for 2 h
  9. customthe solvent was removed
  10. washThe organic layer was washed with saturated aqueous NaHCO3 and brine
  11. dry with materialthen dried over MgSO4
  12. filtrationfiltered
  13. concentrationconcentrated
  14. customThe crude residue was purified by silica column chromatography (15% to 35% EtOAc/Hex)

Quellen und Nachweise

ORD-Eintrag
ord-194d747164b0411eab3b4e548723c4a6
Quelldatensatz
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08822430B2

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