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Water → rac-(1R,2R)-2-(pyridin-2-yl)cyclopropane-1-carboxylic acid

HRID 1774004
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1774004
CON(C)[C:4]([C@@H:6]1[CH2:8][C@H:7]1[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=1)=[O:5].CC(C)([O-:19])C.[K+].O>CCOCC>[N:10]1[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=1[C@@H:7]1[CH2:8][C@H:6]1[C:4]([OH:19])=[O:5]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 962WaterHCID 23665647Potassium tert-butoxide2×HCID 131734716HCID 131734716, Verbindung

Produkt 1

HCID 39235822rac-(1R,2R)-2-(pyridin-2-yl)cyclopropane-1-carboxylic acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Versuchsvorschrift

To a solution of (±)-(trans)-2-pyridin-2-yl-cyclopropanecarboxylic acid methoxy-methyl-amide (950 mg, 4.61 mmol, 1 eq) in Et2O (30 mL), potassium tert-butoxide (569 mg, 5.07 mmol, 1.1 eq) and H2O (0.4 mL) were added. The mixture was stirred at r.t. for 18 hours. Potassium tert-butoxide (1.86 g, 16.6 mmol, 3.6 eq.) was added again. The mixture was stirred at r.t. for 24 hours. The reaction mixture was concentrated in vacuo. The residue was dissolved in water (5 mL) and formic acid (3 mL). The solution was directly purified by prep. HPLC (column: Atlantis, 30×75 mm, 10 um, UV/MS, acidic conditions, extremely polar method) and concentrated in vacuo to give the title compound as a white solid.

Aufarbeitung

  1. stirringThe mixture was stirred at r.t. for 24 hours
  2. concentrationThe reaction mixture was concentrated in vacuo
  3. dissolutionThe residue was dissolved in water (5 mL)
  4. customThe solution was directly purified by prep
  5. concentrationHPLC (column: Atlantis, 30×75 mm, 10 um, UV/MS, acidic conditions, extremely polar method) and concentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-eccd35fc471c470b80d0a99d7eb806b7
Quelldatensatz
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09255090B2

Notizen zur Reaktion

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