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Acetone → 2-(Hydroxymethyl)chroman

HRID 1603870
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1603870
[O:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][CH:2]1[C:11](OCC)=[O:12].[BH4-].[Na+].CC(C)=O>O1CCCC1.O>[O:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][CH:2]1[CH2:11][OH:12]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 180AcetoneHCID 4311764Sodium borohydrideHCID 12909094Ethyl Chroman-2-carboxylate

Produkt 1

HCID 27948162-(Hydroxymethyl)chromanAusbeute 97 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittel2×HCID 8028
Tetrahydrofuran
Lösungsmittel

Versuchsvorschrift

A solution of ethyl 2-chromanecarboxylate (1.575 g, 7.68 mmol) in a mixture of tetrahydrofuran (75 ml) and water (2 ml) was added with sodium borohydride (0.686 g, 18.2 mmol) in small portions and the mixture was left under stirring at room temperature for 48 h. Afterwards the mixture was cooled at -10° C. and added with acetone (47 ml) stirring at room temperature for 0.5 h. Subsequently water (100 ml) was added and the mixture was extracted with dichloromethane. The combined organic phases were dried and the solvent was removed by evaporation under reduced pressure, thereby obtaining 1.218 g of the title product (97% yield).

Aufarbeitung

  1. waitthe mixture was left
  2. temperatureAfterwards the mixture was cooled at -10° C.
  3. stirringstirring at room temperature for 0.5 h
  4. extractionthe mixture was extracted with dichloromethane
  5. customThe combined organic phases were dried
  6. customthe solvent was removed by evaporation under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-97663669672241f8b9a1ce93e4faffd2
Quelldatensatz
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05990142

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