4-(1,3-Dioxolan-2-yl)benzonitrile → HCID 22502706, Verbindung

To a solution of N-methyl-2-methylthiophene-3-carboxamide (18.5 g) in tetrahydrofuran (350 ml) was dropwise added 2.5M n-butyl lithium (100 ml) at −70° C. The resulting solution was stirred at −70° C. for 1.5 hr, followed by the addition of a solution of 4-(1,3-dioxolan-2-yl)benzonitrile (20.9 g) in tetrahydrofuran (100 ml) at once. After the dry ice/acetone bath was removed, the reaction mixture was back to room temperature. Three hours later, an aqueous solution of saturated ammonium chloride was added thereto, and the organic layer was separated, washed with water and dried. The filtrate was concentrated, and the resulting solid was washed with ethyl acetate, tetrahydrofuran/ether and n-hexane in this order. The resulting solid was then dried, to give the title compound as white crystals (6.24 g, yield; 31.7%).

1. customat −70° C
2. customAfter the dry ice/acetone bath was removed
3. customwas back to room temperature
4. additionThree hours later, an aqueous solution of saturated ammonium chloride was added
5. customthe organic layer was separated
6. washwashed with water
7. customdried
8. concentrationThe filtrate was concentrated
9. washthe resulting solid was washed with ethyl acetate, tetrahydrofuran/ether and n-hexane in this order
10. customThe resulting solid was then dried

ORD-Eintrag

ord-ed283addf68e4cee800a57b569581b75

Quelldatensatz

uspto-grants-2005_04

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US06875761B2