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Methanol → 5-Benzyloxypent-2-yl acetate

HRID 1919768
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1919768
[C:1]([O:4][C:5](=[O:7])[CH3:6])(=O)[CH3:2].[CH2:8]([O:15][CH2:16][CH2:17][CH2:18]C(O)C)[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.CO>N1C=CC=CC=1>[C:5]([O:4][CH:1]([CH2:18][CH2:17][CH2:16][O:15][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[CH3:2])(=[O:7])[CH3:6]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 887MethanolHCID 7918Acetic AnhydrideHCID 117455305-(Benzyloxy)pentan-2-ol

Produkt 1

HCID 592348995-Benzyloxypent-2-yl acetateAusbeute 36 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1049PyridineLösungsmittel

Versuchsvorschrift

Acetic anhydride (1.86 mL) was added to a mixed solution of 5-benzyloxypentan-2-ol (957 mg, 4.93 mmol) in pyridine (1.8 mL) in an ice bath. After completion of the reaction, methanol (1.6 mL) was added to the reaction solution in an ice bath, and the solvent was evaporated. The pH was adjusted to 4 with 2 mol/L hydrochloric acid. After extraction with chloroform-water, the organic layer was washed with a saturated sodium chloride solution and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=3:1) to obtain 420 mg of the title compound (yield: 36%) as a colorless oil.

Aufarbeitung

  1. additionwas added to the reaction solution in an ice bath
  2. customthe solvent was evaporated
  3. extractionAfter extraction with chloroform-water
  4. washthe organic layer was washed with a saturated sodium chloride solution
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (hexane:ethyl acetate=3:1)

Quellen und Nachweise

ORD-Eintrag
ord-6412981c89f744c88a57670617327dd6
Quelldatensatz
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08168666B2

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