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Peracetic Acid → HCID 71281752, Verbindung

HRID 1481784
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1481784
[CH2:1]([O:8][C:9]1[N:24]=[CH:23][C:22](I)=[C:21]([O:26][CH2:27][C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[C:10]=1[C:11]([O:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C([Mg]Cl)(C)C.[Li+].[Cl-].B(OC(C)C)(OC(C)C)[O:42]C(C)C.C(OO)(=O)C>C1COCC1.O>[CH2:1]([O:8][C:9]1[N:24]=[CH:23][C:22]([OH:42])=[C:21]([O:26][CH2:27][C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[C:10]=1[C:11]([O:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 6585Peracetic AcidHCID 21531Triisopropyl borateHCID 71281816HCID 71281816, VerbindungHCID 178461733HCID 178461733, Verbindung

Produkt 1

HCID 71281752HCID 71281752, VerbindungAusbeute 36,5 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962
Water
Lösungsmittel
HCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
-45 °C

Versuchsvorschrift

Into a solution of benzyl 2,4-bis(benzyloxy)-5-iodonicotinate (1.0 g, 1.8 mmol) in THF (8.0 mL) at −45° C. was added a solution of i-PrMgCl—LiCl (1.3 M×2.8 mL, 3.6 mmol) dropwise. The mixture was stirred at −45° C. for 30 min, into which triisopropyl borate (0.87 mL, 3.78 mmol) was added dropwise. After stirring at −45° C. for 15 min, the temperature was allowed to rise to room temperature slowly. The mixture was stirred at room temperature for 1.5 h then cooled to −20° C., into which peracetic acid (32%, 0.79 mL, 3.78 mmol) was added. The mixture was stirred at room temperature for another 30 min before it was treated with water (50 mL). The mixture was extracted with ethyl acetate. The organic layers were combined and washed with brine, dried over sodium sulfate, evaporated and purified by silica chromatography (0-30% ethyl acetate in hexanes) to give benzyl 2,4-bis(benzyloxy)-5-hydroxynicotinate (0.29 g, 36%).

Aufarbeitung

  1. additionwas added dropwise
  2. customto rise to room temperature
  3. stirringThe mixture was stirred at room temperature for 1.5 h
  4. additionwas added
  5. stirringThe mixture was stirred at room temperature for another 30 min before it
  6. extractionThe mixture was extracted with ethyl acetate
  7. washwashed with brine
  8. dry with materialdried over sodium sulfate
  9. customevaporated
  10. custompurified by silica chromatography (0-30% ethyl acetate in hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-32f3dc230177495eada0c348f9c4138f
Quelldatensatz
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09409905B2

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