Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641716Generated: November 3, 2026

Water → HCID 57736416, compound

https://huagongshe.com/reaction/1641716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantHCID 57736513HCID 57736513—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
ProductHCID 57736416HCID 5773641640%

Reaction Conditions

Temperature-40 °C

Reaction Steps

A solution of 2-bromo-5-[[(4-chloro-3-methylphenyl)thio](2,5-difluorophenyl) methyl]-4-methylpyridine (2.0 g, 4.4 mmol) in toluene (50 ml) was cooled to −78° C., and in an argon atmosphere, n-butyllithium (1.54 M hexane solution, 3.4 ml, 5.3 mmol) was added thereto. After stirring for 10 minutes at the same temperature, the mixture was allowed to warm to −40° C., stirred for 30 minutes, and cooled again to −78° C., and then N,N-dimethylformamide (409 μl, 5.3 mmol) was added. After stirring for 30 minutes at the same temperature, water was added, and the mixture was extracted twice with ethyl acetate. The combined organic layer was washed with saturated brine, subsequently dried over anhydrous sodium sulfate, and filtered, and then the filtrate was concentrated under reduced pressure. The resulting residue was subjected to flash silica gel column chromatography. The fraction obtained from an elution with hexane:ethyl acetate=95:5 was concentrated under reduced pressure to obtain the title compound (700 mg, 1.7 mmol, 40%) as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114886B2
Source datasetuspto-grants-2012_02
ORD IDord-b2035282bf004dc4add3266c26e3e290
Source noteuspto-grants-2012_02