Borane → 3-(3-Nitrophenyl)propan-1-ol

HRID 1614959Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1614959
[N+:1]([C:4]1[CH:5]=[C:6]([CH2:10][CH2:11][C:12](O)=[O:13])[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2].B>O1CCCC1>[N+:1]([C:4]1[CH:5]=[C:6]([CH2:10][CH2:11][CH2:12][OH:13])[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2]

Komponenten

4

Edukt 2

HCID 6331BoraneHCID 27602243-(3-Nitrophenyl)propionic acid

Produkt 1

HCID 113328423-(3-Nitrophenyl)propan-1-olAusbeute 99,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

3-(3-Nitrophenyl)propanoic acid (3.0 g, 15 mmol) was dissolved in dry tetrahydrofuran (7.6 mL) in a flame-dried flask and cooled in an ice bath. A solution of borane in tetrahydrofuran (20 mL, 20 mmol, 1.0 M) was added dropwise over a period of 30 minutes. The reaction mixture was stirred for an additional 2 hours at rt, then quenched slowly with ice water, and followed by an addition of ether (40 mL). The ether layer was washed with water and saturated aqueous solution of NaHCO3 successively, dried, and concentrated to give the desired product as a yellow gel (2.7 g, 97%).

Aufarbeitung

  1. temperaturecooled in an ice bath
  2. customquenched slowly with ice water
  3. additionfollowed by an addition of ether (40 mL)
  4. washThe ether layer was washed with water and saturated aqueous solution of NaHCO3 successively
  5. customdried
  6. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-c957fe516c334ecbad392a474746ab61
Quelldatensatz
uspto-grants-2014_07
Patentnummer
US08765727B2

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