Water → HCID 54306210, compound

Temperature

0 °C

20.3 g of ethyltriphenylphosphonium iodide was suspended in 160 ml of diethyl ether. Thereto was dropwise added 29.4 ml of 1.5 M n-butyllithium hexane solution, in 2 minutes with stirring at 0° C. Then, the mixture was stirred at 20° C. for 1 hour. To the resulting mixture being maintained at 10°-15° C. was dropwise added a solution of 8.4 g of 4-(2-nitrophenyl)-3-buten-2-one dissolved in 40 ml of diethyl ether, in 30 minutes. The resulting mixture was stirred at 20° C. for 3 hours. Thereto was added 100 ml of water. The organic layer was separated. The aqueous layer was extracted with 100 ml of diethyl ether, and the extract was combined with the previously separated organic layer. The combined solution was washed with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue was purified by column chromatography (eluant: n-hexane/ethyl acetate=5/1) to obtain 3.8 g (yield: 42%) of 1-(3-methyl-1,3-pentadienyl)-2-nitrobenzene as a light yellow oily material.

1. stirringThen, the mixture was stirred at 20° C. for 1 hour
2. temperatureTo the resulting mixture being maintained at 10°-15° C.
3. stirringThe resulting mixture was stirred at 20° C. for 3 hours
4. customThe organic layer was separated
5. extractionThe aqueous layer was extracted with 100 ml of diethyl ether
6. washThe combined solution was washed with an aqueous saturated sodium chloride solution
7. dry with materialdried over anhydrous magnesium sulfate
8. customThe solvent was removed by distillation under reduced pressure
9. customThe residue was purified by column chromatography (eluant: n-hexane/ethyl acetate=5/1)

ORD record

ord-d72a41a053c94a029ecd43037fb1cc66

Source dataset

uspto-grants-1992_11

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05166204