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Triethylamine → 2-(Oxan-2-yl)ethyl methanesulfonate

HRID 1010983
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1010983
[O:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]1[CH2:7][CH2:8][OH:9].C(N(CC)CC)C.[CH3:17][S:18](Cl)(=[O:20])=[O:19].C(=O)(O)[O-].[Na+]>C(Cl)Cl>[CH3:17][S:18]([O:9][CH2:8][CH2:7][CH:2]1[CH2:3][CH2:4][CH2:5][CH2:6][O:1]1)(=[O:20])=[O:19]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 8471TriethylamineHCID 31297Methanesulfonyl chlorideHCID 516892Sodium BicarbonateHCID 139481282-(Oxan-2-yl)ethan-1-ol

Produkt 1

HCID 576998282-(Oxan-2-yl)ethyl methanesulfonateAusbeute 110 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344
Dichloromethane
Lösungsmittel

Versuchsvorschrift

2-(Tetrahydro-2H-pyran-2-yl)ethanol (465 mg) was dissolved in dry DCM (10 mL) and triethylamine (996 mg) was added. The stirred solution was cooled in an ice bath under nitrogen and methanesulphonyl chloride (359 mg) was added dropwise over 5 mins. The reaction was allowed to warm to room temperature as the ice bath melted and was left for 16 h. The mixture was then shaken with saturated sodium bicarbonate solution and the aqueous layer was extracted with DCM (×2). The combined organic extracts were washed with brine, dried using a hydrophobic frit and evaporated to give the title compound as a brown oil (718 mg).

Aufarbeitung

  1. temperatureThe stirred solution was cooled in an ice bath under nitrogen
  2. extractionthe aqueous layer was extracted with DCM (×2)
  3. washThe combined organic extracts were washed with brine
  4. customdried
  5. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-355400d2f3d942ef96adb9d895679797
Quelldatensatz
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07977344B2

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