2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 57428834, Verbindung

Temperatur

-78 °C

nBuLi (1.1 mL, 1.6 M solution in hexane, 1.8 mmol) was added to a stirred solution of 2,3-dibromo-5-chlorothiophene (0.50 g, 1.8 mmol) in 10 mL of THF at −78° C. The solution was stirred for 10 min at −78° C. before 0.35 g (1.8 mmol) of 5-bromo-2-chloropyrimidine was added. The reaction solution was stirred for 30 min at −78° C., then quenched by addition of 1 mL of AcOH in 4 mL of MeOH. Solid 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (0.82 g, 3.6 mmol) was added and the reaction mixture warmed to 0° C. and stirred for 10 min. The reaction mixture was then poured into 50 mL of a 0.5 M solution of sodium ascorbate and diluted with 100 mL of a 1 M aqueous solution of Na2CO3. The aqueous solution was extracted four times with CH2Cl2 and the combined organic extracts dried over MgSO4, filtered and concentrated to give the crude product which was purified by flash chromatography eluting with a linear gradient of 50% EtOAc in hexane to neat EtOAc, then to 20% MeOH in EtOAc to deliver the title compound. MS (M+H)+ 389.

1. additionwas added
2. customquenched by addition of 1 mL of AcOH in 4 mL of MeOH
3. temperaturethe reaction mixture warmed to 0° C.
4. stirringstirred for 10 min
5. extractionThe aqueous solution was extracted four times with CH2Cl2
6. dry with materialthe combined organic extracts dried over MgSO4
7. filtrationfiltered
8. concentrationconcentrated

ORD-Eintrag

ord-3ca00070861d4269a1a47f8fdc13fc23

Quelldatensatz

uspto-grants-2010_12

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07858785B2