(Dimethyl sulfide)trihydroboron → 2,3-Difluoro-4-(2-hydroxyethyl)phenol

HRID 1689396

Reaktionsgleichung

Reaktionsgleichung von HRID 1689396
CSC.B.[F:5][C:6]1[C:11]([F:12])=[C:10]([OH:13])[CH:9]=[CH:8][C:7]=1[CH2:14][C:15](O)=[O:16]>O1CCCC1>[F:12][C:11]1[C:6]([F:5])=[C:7]([CH2:14][CH2:15][OH:16])[CH:8]=[CH:9][C:10]=1[OH:13]

Komponenten

4

Edukt 2

HCID 12423031(Dimethyl sulfide)trihydroboronHCID 299221072-(2,3-Difluoro-4-hydroxyphenyl)acetic acid

Produkt 1

HCID 534161452,3-Difluoro-4-(2-hydroxyethyl)phenol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

A solution of borane dimethylsulfide complex (2M in THF, 14.4 mL) was added dropwise to a solution of 2-(2,3-difluoro-4-hydroxyphenyl)acetic acid (example 77, step a) (1.08 g) in tetrahydrofuran (25 mL) at 0° C. and the resulting mixture was allowed to warm to RT and stirred overnight. The reaction was quenched with methanol and when bubbling had ceased the solvent evaporated. The residue was purified by silica gel chromatography eluting with 4:1 isohexane:ethyl acetate to ethyl acetate gradient. The fractions containing product were combined and evaporated to give the subtitled compound as white solid. Yield 0.95 g.

Aufarbeitung

  1. customThe reaction was quenched with methanol and when
  2. custombubbling
  3. customevaporated
  4. customThe residue was purified by silica gel chromatography
  5. washeluting with 4:1 isohexane
  6. additionThe fractions containing product
  7. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-4d3caea8e3284c38a3665431d788b75d
Quelldatensatz
uspto-grants-2012_04
Patentnummer
US08148373B2

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