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Hydrogen Peroxide → (1R,3R)-methyl 1-(benzyloxycarbonylamino)-3-(4-(2-hydroxyethyl)phenyl)cyclopentanecarboxylate

HRID 1511866
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1511866
B1C2CCCC1CCC2.[CH2:10]([O:17][C:18]([NH:20][C@:21]1([C:34]([O:36][CH3:37])=[O:35])[CH2:25][CH2:24][C@@H:23]([C:26]2[CH:31]=[CH:30][C:29]([CH:32]=[CH2:33])=[CH:28][CH:27]=2)[CH2:22]1)=[O:19])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.B([O-])[O-:39].[OH-].[Na+].OO>C1COCC1>[CH2:10]([O:17][C:18]([NH:20][C@:21]1([C:34]([O:36][CH3:37])=[O:35])[CH2:25][CH2:24][C@@H:23]([C:26]2[CH:27]=[CH:28][C:29]([CH2:32][CH2:33][OH:39])=[CH:30][CH:31]=2)[CH2:22]1)=[O:19])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 5

HCID 784Hydrogen PeroxideHCID 14798Sodium HydroxideHCID 789669-Borabicyclo(3.3.1)nonaneHCID 57554635(1R,3R)-methyl 1-(benzyloxycarbonylamino)-3-(4-vinylphenyl)cyclopentanecarboxylateHCID 178514824HCID 178514824, Verbindung

Produkt 1

HCID 57554629
(1R,3R)-methyl 1-(benzyloxycarbonylamino)-3-(4-(2-hydroxyethyl)phenyl)cyclopentanecarboxylate
Ausbeute 71 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

9-BBN (25 ml, 12.50 mmol) was added dropwise to a stirred and cooled solution of (1R,3R)-methyl 1-(benzyloxycarbonylamino)-3-(4-vinylphenyl)cyclopentanecarboxylate (0.682 g, 1.797 mmol) in THF (15 mL). The reaction mixture was checked by TLC to ensure complete conversion to boronate. Once complete the ice bath was removed and stirring was continued overnight. The reaction mixture was cooled to 0° C. and methanol (20 ml) was added. Aqueous NaOH (7.30 ml, 14.59 mmol) and H2O2 (1.522 ml, 14.90 mmol) were poured into the reaction mixture. Stirring was continued for 2 hours. The solvent was removed under reduced pressure and the product purified by FCC to afford (1R,3R)-methyl 1-(benzyloxycarbonylamino)-3-(4-(2-hydroxyethyl)phenyl)cyclopentanecarboxylate (0.507 g, 1.276 mmol, 71.0% yield) as colorless oil.

Aufarbeitung

  1. customOnce complete the ice bath was removed
  2. stirringstirring
  3. additionmethanol (20 ml) was added
  4. stirringStirring
  5. waitwas continued for 2 hours
  6. customThe solvent was removed under reduced pressure
  7. customthe product purified by FCC

Quellen und Nachweise

ORD-Eintrag
ord-9c2891a94cdb4a66bc71acb7475415ad
Quelldatensatz
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08217027B2

Notizen zur Reaktion

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