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4-Iodotoluene → Tolylboronic acid

HRID 49420
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 49420
I[C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][CH:3]=1.C([Li])CCC.C([O:18][B:19](OCCCC)[O:20]CCCC)CCC>C(OCC)C>[CH3:8][C:5]1[CH:6]=[CH:7][C:2]([B:19]([OH:20])[OH:18])=[CH:3][CH:4]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 122074-IodotolueneHCID 12712Tributyl borateHCID 178418339Butyllithium

Produkt 1

HCID 79799Tolylboronic acidAusbeute 85,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a solution of 4-iodotoluene (35 g, 160.5 mmol) in diethyl ether (400 mL) was added n-butyllithium (2 M in pentane, 88.3 mL, 176.6 mmol) at 0° C. After stirring at 0° C. for another 15 min the solution was cooled to −60° C. and tributylborate (60.6 mL, 224.7 mmol) was added. The cooling bath was removed and the reaction allowed to heat up to room temperature. The solution was acidified with hydrochloric acid (2 N, 280 mL) and the organic phase separated off. The aqueous phase was extracted with diethyl ether 2×125 mL). The combined organic phases were extracted with sodium hydroxide (1 N, 5×50 mL). The combined aqueous extracts were acidified to give 18.6 g of the desired material.

Aufarbeitung

  1. temperaturewas cooled to −60° C.
  2. customThe cooling bath was removed
  3. temperatureto heat up to room temperature
  4. customthe organic phase separated off
  5. extractionThe aqueous phase was extracted with diethyl ether 2×125 mL)
  6. extractionThe combined organic phases were extracted with sodium hydroxide (1 N, 5×50 mL)

Quellen und Nachweise

ORD-Eintrag
ord-74803c53f6274e458b772a5e05af20cd
Quelldatensatz
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06706749B2

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