Hydrochloric Acid → HCID 23016515、化合物

Under nitrogen atmosphere, 11.7 ml of n-butyllithium (1.57 M-n-hexane solution) was dropwise added at −20° C. to a mixture of 1.85 g of diisopropylamine and 50 ml of tetrahydrofuran, and then the mixture was stirred at the same temperature for 30 minutes. 5.0 g of 6-bromo-2,2,3,3,-tetrafluoro-1,4-benzodioxane was dropwise added thereto at a temperature of at most −50° C., followed by stirring at the same temperature for 30 minutes. Then, 5.5 ml of methyl iodide was dropwise added thereto at a temperature of at most −70° C., and then the temperature was raised to room temperature, followed by a reaction for 15 hours. After completion of the reaction, the reaction mixture was put into water and then weakly acidified by an addition of hydrochloric acid. Then, the mixture was extracted with ethyl ether, and the extract was washed with water and dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: n-hexane) to obtain 3.40 g of oily 6-bromo-2,2,3,3,-tetrafluoro-5-methyl-1,4-benzodioxane. The NMR spectrum data of this product were as follows.

1. customat a temperature of at most −50° C.
2. stirringby stirring at the same temperature for 30 minutes
3. customfollowed by a reaction for 15 hours
4. customAfter completion of the reaction
5. extractionThen, the mixture was extracted with ethyl ether
6. washthe extract was washed with water
7. dry with materialdried over magnesium sulfate
8. concentrationfollowed by concentration under reduced pressure
9. customThe obtained residue was purified by silica gel column chromatography (eluent: n-hexane)

ORDレコード

ord-883b255546f94fe0914f0a392d828043

出典データセット

uspto-grants-2010_03

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07683096B2