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Methyl iodide → (2,2-Difluoro-7-methyl-1,3-benzodioxol-4-yl)boronic acid

HRID 527655
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 527655
[F:1][C:2]1([F:14])[O:6][C:5]2[CH:7]=[CH:8][CH:9]=[C:10]([B:11]([OH:13])[OH:12])[C:4]=2[O:3]1.[Li][CH:16](CC)C.C1CCCCC1.CI>C1COCC1>[F:14][C:2]1([F:1])[O:6][C:5]2[C:7]([CH3:16])=[CH:8][CH:9]=[C:10]([B:11]([OH:13])[OH:12])[C:4]=2[O:3]1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 6328Methyl iodideHCID 8078CyclohexaneHCID 16427145(2,2-Difluoro-1,3-dioxaindan-4-yl)boronic acid2×HCID 178418400CID 53628100

Produkt 1

HCID 86698459(2,2-Difluoro-7-methyl-1,3-benzodioxol-4-yl)boronic acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028
Tetrahydrofuran
Lösungsmittel

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

(2,2-difluoro-1,3-benzodioxol-4-yl)boronic acid (Intermediate 195, crude material) was dissolved in THF (20 mL) and the resulting solution cooled down to −78° C. sec-BuLi 1.4M solution in cyclohexane (17.4 ml, 24.36 mmol) was added dropwise and the reaction mixture was stirred for 1.5 hours at −78° C. Methyl iodide (4.6 ml, 73 mmol) was then added and the reaction mixture was stirred for 2 hours while the temperature was allowed to reach room temperature. The reaction was quenched by addition of an aqueous 2N solution of HCl and diluted with ethyl acetate. The organic layer was collected and then washed twice with brine, dried over Na2SO4 and evaporated to dryness. Crystallization from n-heptane afforded the title compound (150 mg) as white solid.

Aufarbeitung

  1. additionwas added dropwise
  2. stirringthe reaction mixture was stirred for 2 hours while the temperature
  3. customto reach room temperature
  4. customThe reaction was quenched by addition of an aqueous 2N solution of HCl
  5. additiondiluted with ethyl acetate
  6. customThe organic layer was collected
  7. washwashed twice with brine
  8. dry with materialdried over Na2SO4
  9. customevaporated to dryness
  10. customCrystallization from n-heptane

Quellen und Nachweise

ORD-Eintrag
ord-d2f505d1d255450a8c5eb99f499f23f2
Quelldatensatz
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09346790B2

Notizen zur Reaktion

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