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(Dimethyl sulfide)trihydroboron → 2-(3-(Bromomethyl)-5-chlorophenyl)ethanol

HRID 446367
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 446367
CSC.B.[Br:5][CH2:6][C:7]1[CH:8]=[C:9]([CH2:14][C:15](O)=[O:16])[CH:10]=[C:11]([Cl:13])[CH:12]=1>C1COCC1>[Br:5][CH2:6][C:7]1[CH:8]=[C:9]([CH2:14][CH2:15][OH:16])[CH:10]=[C:11]([Cl:13])[CH:12]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 12423031(Dimethyl sulfide)trihydroboronHCID 579893592-(3-(Bromomethyl)-5-chlorophenyl)acetic acid

Produkt 1

HCID 579892922-(3-(Bromomethyl)-5-chlorophenyl)ethanol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

A solution of borane dimethyl sulfide complex (2M in THF, 2.8 mL) was added portionwise over 5 minutes to a solution of 2-(3-(bromomethyl)-5-chlorophenyl)acetic acid [Aromatic Intermediate 8, step a] (0.73 g) in dry THF (10 mL) at room temperature. The resulting effervescing solution was stirred for 1 hour, then cooled in ice-water and quenched by the portionwise addition of methanol (3 mL) over 5 minutes. The solution was stirred at room temperature for a further 20 minutes and then concentrated in vacuo. The residue was purified by flash chromatography on silica eluted with 25% ethyl acetate in isohexane to afford the crude subtitled compound as a white solid. Yield 0.46 g.

Aufarbeitung

  1. customquenched by the portionwise addition of methanol (3 mL) over 5 minutes
  2. stirringThe solution was stirred at room temperature for a further 20 minutes
  3. concentrationconcentrated in vacuo
  4. customThe residue was purified by flash chromatography on silica
  5. washeluted with 25% ethyl acetate in isohexane

Quellen und Nachweise

ORD-Eintrag
ord-59e97bea4b9f4e27ae072f6c45e03852
Quelldatensatz
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08476265B2

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