Hydrochloric Acid → HCID 86661430, compound

Temperature

-40 °C

5.00 g (98% by weight; 19.0 mmol) of 3-fluoro-4-(pentafluoroethyl)benzoic acid were introduced into 40 ml of dry tetrahydrofuran. 4.73 g (40.7 mmol) of 1,2-bis-(dimethylamino)ethane were added, and the mixture was then cooled to −40° C. Then 16.3 ml of a 2.5 M solution (40.7 mmol) of n-butyllithium in hexane were added dropwise at a rate such that the temperature was in a range from −33° C. to −35° C. The contents were stirred at −35° C. for 4 hours. Then a solution of 8.25 g (58.1 mmol) of iodomethane in 10 ml of dry THF was added dropwise, and the mixture was stirred at −35° C. for 1 hour. Thereafter the contents were warmed to room temperature (RT) and stirred at this temperature for 16 hours. For working up, 50 ml of 2M hydrochloric acid were cautiously added, and then the aqueous phase was extracted with diethyl ether. The combined organic phases were dried and freed from the solvents. The residue was stirred in n-heptane and subsequently filtered. This gave 2.33 g of residue as a clean product. The filtrate was freed from the solvent, and the residue was again stirred in n-heptane. Filtration produced 590 mg of residue, which was identified as a product with a purity of 70% by weight.

1. customwas in a range from −33° C. to −35° C
2. stirringthe mixture was stirred at −35° C. for 1 hour
3. temperatureThereafter the contents were warmed to room temperature (RT)
4. stirringstirred at this temperature for 16 hours
5. extractionthe aqueous phase was extracted with diethyl ether
6. customThe combined organic phases were dried
7. stirringThe residue was stirred in n-heptane
8. filtrationsubsequently filtered
9. stirringthe residue was again stirred in n-heptane
10. filtrationFiltration

ORD record

ord-592a9188abb1467f896bbefda2dd3265

Source dataset

uspto-grants-2013_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08536097B2