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(Dimethyl sulfide)trihydroboron → 2-(2-Chloro-3-(hydroxymethyl)phenyl)ethanol

HRID 471184
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 471184
B.CSC.[C:5]([CH2:8][C:9]1[C:10]([Cl:18])=[C:11]([CH:15]=[CH:16][CH:17]=1)[C:12](O)=[O:13])(O)=[O:6]>C1COCC1>[Cl:18][C:10]1[C:11]([CH2:12][OH:13])=[CH:15][CH:16]=[CH:17][C:9]=1[CH2:8][CH2:5][OH:6]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 12423031(Dimethyl sulfide)trihydroboronHCID 579889673-(Carboxymethyl)-2-chlorobenzoic acid

Produkt 1

HCID 579892482-(2-Chloro-3-(hydroxymethyl)phenyl)ethanol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

A solution of borane-methyl sulfide complex (2M in THF, 20 mL) was added portionwise over 5 minutes to a suspension of 3-(carboxymethyl)-2-chlorobenzoic acid (example 80, step b) (4.11 g) in dry THF (100 mL) at room temperature. The resulting effervescing suspension was stirred at room temperature for 30 minutes, then heated to reflux for 60 minutes, and allowed to cool to room temperature overnight. The mixture was quenched by the portionwise addition of methanol (15 mL) over 15 minutes. The mixture was diluted further with methanol to give a solution, which was then concentrated in vacuo to give a syrup. The syrup was purified by flash chromatography on silica eluted with 2% methanol in dichloromethane to the afford the crude subtitled compound as a white solid. Yield 1.44 g.

Aufarbeitung

  1. temperatureheated
  2. temperatureto reflux for 60 minutes
  3. temperatureto cool to room temperature overnight
  4. customThe mixture was quenched by the portionwise addition of methanol (15 mL) over 15 minutes
  5. additionThe mixture was diluted further with methanol
  6. customto give a solution, which
  7. concentrationwas then concentrated in vacuo
  8. customto give a syrup
  9. customThe syrup was purified by flash chromatography on silica
  10. washeluted with 2% methanol in dichloromethane to the

Quellen und Nachweise

ORD-Eintrag
ord-18378592b1a34f529405b56eb595f303
Quelldatensatz
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08629271B2

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