Methyl iodide → 1-(4-Cyanophenyl)-2-methylhydrazine

To a mixture of 260 g of (1-(4-cyanophenyl)-2-methylhydrazino)triphenylphosphonium bromide and 2,000 ml of tetrahydrofuran, 347 ml of n-butyllithium (1.66 M, hexane solution) was added at 0° C., and the resulting mixture was stirred at room temperature for 1 hour. 85.6 g of methyl iodide was added thereto, and the resulting mixture was stirred for 20 hours. Then, 1,400 ml of 2N aqueous sodium hydroxide was added. The mixture was stirred at 50° C. for another 1 hour. After the mixture was allowed to separate, the aqueous layer was extracted with benzene. The organic layers were combined and extracted with 1N hydrochloric acid, and the extract was washed with chloroform. The resulting acidic aqueous solution was adjusted to pH 10-12 with 2N aqueous sodium hydroxide and then extracted with benzene. The extract was washed with saturated aqueous sodium chloride and dried over anhydrous sodium sulfate. After the insolubles were filtered off, the solvent was removed by evaporation under reduced pressure to leave 60.8 g of the title compound as a pale yellow liquid.

1. additionwas added at 0° C.
2. stirringthe resulting mixture was stirred for 20 hours
3. stirringThe mixture was stirred at 50° C. for another 1 hour
4. customto separate
5. extractionthe aqueous layer was extracted with benzene
6. extractionextracted with 1N hydrochloric acid
7. washthe extract was washed with chloroform
8. extractionextracted with benzene
9. washThe extract was washed with saturated aqueous sodium chloride
10. dry with materialdried over anhydrous sodium sulfate
11. filtrationAfter the insolubles were filtered off
12. customthe solvent was removed by evaporation under reduced pressure

ORDレコード

ord-9b7a18c2138643ad944a8e6cd86685f1

出典データセット

uspto-grants-1999_10

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05968967