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

HRID 471066
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 471066
B.CSC.[Br:5][CH2:6][C:7]1[CH:8]=[C:9]([CH2:14][C:15](O)=[O:16])[CH:10]=[C:11]([F: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]([F:13])[CH:12]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 12423031(Dimethyl sulfide)trihydroboronHCID 579890372-(3-(Bromomethyl)-5-fluorophenyl)acetic acid

Produkt 1

HCID 579893452-(3-(Bromomethyl)-5-fluorophenyl)ethanol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Borane-methyl sulfide complex (2M in THF, 17.4 mL) was added dropwise over 10 minutes to a solution of 2-(3-(bromomethyl)-5-fluorophenyl)acetic acid (example 41, step a) (4.3 g) in THF (60 mL) at 0° C. The mixture was stirred at 0° C. for 10 minutes and then at 20° C. for 1 hour. The reaction mixture was quenched by dropwise addition of methanol and the solvents were removed under reduced pressure. The crude product was purified by flash silica chromatography using 30% ethyl acetate in isohexane as solvent. Pure fractions were evaporated to dryness to afford the subtitled compound. Yield 3.7 g.

Aufarbeitung

  1. waitat 20° C. for 1 hour
  2. customThe reaction mixture was quenched by dropwise addition of methanol
  3. customthe solvents were removed under reduced pressure
  4. customThe crude product was purified by flash silica chromatography
  5. customPure fractions were evaporated to dryness

Quellen und Nachweise

ORD-Eintrag
ord-1cc3d7c6adf74dacbdfcf29d316655b4
Quelldatensatz
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08629271B2

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