Furfuryl Alcohol → Methanesulfonic acid furan-2-ylmethyl ester

HRID 1693639Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1693639
[O:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][OH:7].C(N(CC)CC)C.[CH3:15][S:16](Cl)(=[O:18])=[O:17]>C(Cl)Cl>[CH3:15][S:16]([O:7][CH2:6][C:2]1[O:1][CH:5]=[CH:4][CH:3]=1)(=[O:18])=[O:17]

Komponenten

5

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To the solution of furan-2-ylmethanol (500 mg, 5.1 mmol) in CH2Cl2 (10 mL) and triethylamine (1.54 g, 15.3 mmol) at 0° C. was added dropwise methanesulfonyl chloride (695 mg, 6.1 mmol). The mixture was stirred at 0° C. for 15 min and was quenched with 10 mL of water. The layers were separated and the aqueous layer was extracted with CH2Cl2 (1×10 mL). The combined organic extracts were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure to afford the title compound.

Aufarbeitung

  1. customwas quenched with 10 mL of water
  2. customThe layers were separated
  3. extractionthe aqueous layer was extracted with CH2Cl2 (1×10 mL)
  4. dry with materialThe combined organic extracts were dried over anhydrous Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-e49580dd74364160a354a59d3be2d06e
Quelldatensatz
uspto-grants-2012_04
Patentnummer
US08158663B2

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