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Tyramine → 4-Vinylacetamidoethyl phenol

HRID 11730
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 11730
[NH2:1][CH2:2][CH2:3][C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[CH:6][CH:5]=1.C(N(CC)CC)C.[CH:18]([CH2:20][C:21](Cl)=[O:22])=[CH2:19]>C(Cl)Cl>[CH:18]([CH2:20][C:21]([NH:1][CH2:2][CH2:3][C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[CH:6][CH:5]=1)=[O:22])=[CH2:19]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 5610TyramineHCID 8471TriethylamineHCID 10975427But-3-enoyl Chloride

Produkt 1

HCID 626796864-Vinylacetamidoethyl phenolAusbeute 80 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

A 1000 mL 3-neck, round bottom flask connected with a reflux condenser and a drying tube, is charged with 250 mL of methylene chloride, 5.48 grams (0.04 mole) 4-aminoethylphenol and 4.04 grams (0.04 mole) triethylamine. The contents are chilled with an ice bath. Through a dropping funnel, 4.18 grams (0.04 mole) of vinylacetyl chloride is added into the flask over a period of 30 minutes. The ice bath is then removed and the contents are continuously stirred overnight. The mixture is then filtered and then condensed using a rotavapor. HPLC analysis indicates only one major product. The product is then passed through silica gel chromatography to give a final purified product with a yield of at least 80 percent. The product is identified by NMR and Mass Spectroscopy.

Aufarbeitung

  1. customA 1000 mL 3-neck, round bottom flask connected with a reflux condenser and a drying tube
  2. temperatureThe contents are chilled with an ice bath
  3. customThe ice bath is then removed
  4. filtrationThe mixture is then filtered
  5. customcondensed
  6. customto give
  7. customa final purified product with a yield of at least 80 percent

Quellen und Nachweise

ORD-Eintrag
ord-e731d9e07c514ef2b02efd3f861e74ea
Quelldatensatz
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07098283B2

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