Methyl iodide → 5-bromo-1,3-difluoro-2-methylbenzene

To a solution of 2.04 g of diisopropylamine in 30 ml of tetrahydrofuran is dropwise added 9.19 ml of 1.6 M n-hexane solution of n-butyllithium at -20° C. At the same temperature, the resulting mixture is stirred for one hour and then cooled to -70° C., at which temperature a solution of 3 g of 3,5-difluorobromobenzene in 10 ml of tetrahydrofuran is dropwise added thereto over 30 minutes. The temperature of the resulting reaction mixture is elevated to -40° C. and then lowered again to -70° C., at which temperature 0.97 ml of methyl iodide is then added thereto. The temperature of the resulting mixture is elevated to room temperature, and 80 ml of water and 80 ml of ethyl acetate are then added thereto, after which the resulting organic layer is separated, washed successively with water and a saturated saline solution and then dried over anhydrous magnesium sulfate. Thereafter, the solvent is removed from the thus dried layer by distillation under reduced pressure. The residue obtained is purified by a column chromatography [eluent:hexane:ethyl acetate=10:1], to obtain 1.98 g of colorless, oily 4-bromo-2,6-difluorotoluene.

1. customat -20° C
2. additionis dropwise added
3. waitover 30 minutes
4. customThe temperature of the resulting reaction mixture
5. customis elevated to -40° C.
6. additionis then added
7. customis elevated to room temperature
8. customafter which the resulting organic layer is separated
9. washwashed successively with water
10. dry with materiala saturated saline solution and then dried over anhydrous magnesium sulfate
11. customThereafter, the solvent is removed from the thus dried layer by distillation under reduced pressure
12. customThe residue obtained
13. customis purified by a column chromatography [eluent:hexane:ethyl acetate=10:1]

ORDレコード

ord-6e0de5d68d5e482698c4c4a474d44014

出典データセット

uspto-grants-1999_08

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05932620