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Tin tetrachloride → 3-[2-Azido-2-(2-hydroxyethoxy)ethoxy]benzoic acid ethyl ester

HRID 661191
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 661191
[CH2:1]([O:3][C:4](=[O:18])[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([O:11][CH2:12][CH:13]2[O:17][CH2:16][CH2:15][O:14]2)[CH:6]=1)[CH3:2].[N:19]([Si](C)(C)C)=[N+:20]=[N-:21].Cl[Sn](Cl)(Cl)Cl>CO>[CH2:1]([O:3][C:4](=[O:18])[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([O:11][CH2:12][CH:13]([N:19]=[N+:20]=[N-:21])[O:14][CH2:15][CH2:16][OH:17])[CH:6]=1)[CH3:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 24287Tin tetrachlorideHCID 78378AzidotrimethylsilaneHCID 17999177Ethyl 3-((1,3-dioxolan-2-yl)methoxy)benzoate

Produkt 1

HCID 597717683-[2-Azido-2-(2-hydroxyethoxy)ethoxy]benzoic acid ethyl ester

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

To a mixture of 3-([1,3]-dioxolan-2-ylmethoxy)-benzoic acid ethylester (2.02 g, 8 mmol) and azidotrimethylsilane (1.17 ml, 8.8 mmol) was added SnCl4 (60 μl) at room temperature under nitrogen. After 2 hr, 2% aqueous methanol (10 ml) was added to the reaction mixture and the reaction was stirred at room temperature for 30 minutes. All the solvents were evaporated under reduced pressure. The residue was co-evaporated with ethanol (2×10 ml). The residue was purified by a column chromatography (3×20 cm). The product was eluted with 0 to 1% methanol in DCM. The title compound was obtained as a colourless oil (2.01 g, 85.1%). APCI-MS, m/z 267.90 (M−N2+1).

Aufarbeitung

  1. customAll the solvents were evaporated under reduced pressure
  2. customThe residue was purified by a column chromatography (3×20 cm)
  3. washThe product was eluted with 0 to 1% methanol in DCM

Quellen und Nachweise

ORD-Eintrag
ord-385816a1286b40f691afd9913414c636
Quelldatensatz
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08084590B2

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