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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13220Generated: October 26, 2026

2,4-Difluorophenol → (S)-benzyl 4-(2,4-difluorophenoxy)-3-oxobutan-2-ylcarbamate

https://huagongshe.com/reaction/13220

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DifluorophenolHCID 123051—
ReactantPotassium FluorideHCID 522689—
Reactant(S)-benzyl 4-bromo-3-oxobutan-2-ylcarbamateHCID 15485144—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product(S)-benzyl 4-(2,4-difluorophenoxy)-3-oxobutan-2-ylcarbamateHCID 5933987494.2%

Reaction Steps

A mixture of (S)-benzyl 4-bromo-3-oxobutan-2-ylcarbamate (prepared according to R. V. Hoffman et al., J. Org. Chem. 2001, 66, 5790-5795) (600 mg, 2.00 mmol), 2,4-difluorophenol (312 mg, 2.40 mmol) and potassium fluoride (380 mg, 6.54 mmol) in DMF (4 mL) was stirred at r.t. for 17 h. Water (15 mL) and dichloromethane (3 mL) were added and the mixture was stirred for 30 min. The mixture was added to a phase separator. The water phase was once more stirred with dichloromethane (3 mL), and added to the phase separator. The organic phases were concentrated and the residue was purified by flash chromatography on silica gel (cyclohexane/ethyl acetate 3/1) to give the title compound as a white solid (658 mg, 94% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728030B2
Source datasetuspto-grants-2010_06
ORD IDord-fe4251190ce44f28a6e56c60c003be12
Source noteuspto-grants-2010_06