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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095828Generated: October 31, 2026

Potassium tert-butoxide → HCID 58158560, compound

https://huagongshe.com/reaction/2095828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 58158465HCID 58158465—
SolventDimethylformamideHCID 6228—
ProductHCID 58158560HCID 5815856039%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 1-(3-bromobutyl)-3-(4-fluorophenyl)urea (1750 mg, 6.1 mmol) in N,N-dimethylformamide (30 mL) was added potassium tert-butoxide (920 mg, 7.0 mmol), and the mixture was stirred at 50° C. for 6 hr. The solvent was evaporated under reduced pressure, and ethyl acetate/tetrahydrofuran and 6N aqueous hydrochloric acid solution were added to the residue. The aqueous layer was extracted with ethyl acetate/tetrahydrofuran (×3). The combined organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (NH silica gel, ethyl acetate/hexane=50/50→100/0) to give the title compound (490 mg, 39%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445509B2
Source datasetuspto-grants-2013_05
ORD IDord-2feaca9eab3f40b29623361b67685c8d
Source noteuspto-grants-2013_05