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Morpholine → 4-(3-Nitrobenzyl)morpholine

HRID 255036
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 255036
Br[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([N+:9]([O-:11])=[O:10])[CH:4]=1.[NH:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1.C(N(CC)CC)C>C1COCC1>[N+:9]([C:5]1[CH:4]=[C:3]([CH:8]=[CH:7][CH:6]=1)[CH2:2][N:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1)([O-:11])=[O:10]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 8083MorpholineHCID 8471TriethylamineHCID 77568Benzene, 1-(bromomethyl)-3-nitro-

Produkt 1

HCID 7832314-(3-Nitrobenzyl)morpholineAusbeute 94 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

A solution of 1-bromomethyl-3-nitrobenzene (2.16 g, 10 mmol), morpholine (1.76 g, 20.2 mmol) and triethylamine (1.0 mL) in THF (60 mL) was heated for two hours at 60° C. The solvent was evaporated, water was added and the product was isolated by extraction with ether. The ether extract was dried over Mg2SO4 and the solvent was evaporated. The crystalline residue was used in the next step without further purification. The product, 4-(3-nitrobenzyl)morpholine, was obtained in 94% yield (2.09 g).

Aufarbeitung

  1. customThe solvent was evaporated
  2. additionwater was added
  3. customthe product was isolated by extraction with ether
  4. extractionThe ether extract
  5. dry with materialwas dried over Mg2SO4
  6. customthe solvent was evaporated
  7. customThe crystalline residue was used in the next step without further purification

Quellen und Nachweise

ORD-Eintrag
ord-b9fde5b032db4a4e86c6f0cfbdde9e71
Quelldatensatz
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07875728B2

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