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Ethylene Oxide → 2-[(3R)-3-methoxymethylmorpholino]ethanol

HRID 1765983
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1765983
Cl.[CH3:2][O:3][CH2:4][C@@H:5]1[CH2:10][O:9][CH2:8][CH2:7][NH:6]1.C(N(CC)CC)C.[CH2:18]1[O:20][CH2:19]1>CO.C1(C)C=CC=CC=1>[CH3:2][O:3][CH2:4][C@H:5]1[N:6]([CH2:18][CH2:19][OH:20])[CH2:7][CH2:8][O:9][CH2:10]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 6354Ethylene OxideHCID 8471TriethylamineHCID 53338712(3R)-3-(Methoxymethyl)morpholine--hydrogen chloride (1/1)

Produkt 1

HCID 538274862-[(3R)-3-methoxymethylmorpholino]ethanol

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 887MethanolLösungsmittelHCID 1140
Toluene
Lösungsmittel

Versuchsvorschrift

To a mixed solution of (3R)-3-(methoxymethyl)morpholine hydrochloride (4.71 g) and triethylamine (4.11 ml) in methanol (110 ml) was added 5.8 M ethylene oxide (22 ml) in toluene solution at room temperature. After stirring the reaction mixture at the same temperature for 2 days, the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography using a mixed solvent of dichloromethane and methanol (20:1). Fractions containing the desired compound were collected and the solvent was evaporated under reduced pressure to give 2-[(3R)-3-(methoxymethyl)morpholino]ethanol (4.67 g) in the form of an oily substance.

Aufarbeitung

  1. customthe solvent was evaporated under reduced pressure
  2. customThe residue was purified by silica gel column chromatography
  3. additionFractions containing the desired compound
  4. customwere collected
  5. customthe solvent was evaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-faa5b360b8f441e083516017d2284790
Quelldatensatz
uspto-grants-2007_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07229992B2

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