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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743668Generated: October 31, 2026

tert-Butyl bromoacetate → tert-Butyl 4-(2,6-difluorophenyl)-4-oxobutyrate

https://huagongshe.com/reaction/1743668

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl bromoacetateHCID 79177—
Reactant1-(2,6-Difluorophenyl)ethan-1-oneHCID 83643—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Solvent2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
Producttert-Butyl 4-(2,6-difluorophenyl)-4-oxobutyrateHCID 21964547—

Reaction Conditions

Temperature-60 °C

Reaction Steps

To a stirred solution of 2,6-Difluoroacetophenone (5 g, 32 mmol) in dry THF (40 ml) and DMPU (8 ml) was added a solution of lithium bis(trimethylsilyl)amide (1.0M, 45 ml) at −60° C. under argon. After stirring for 10 minutes at −60° C., tert-Butyl bromoacetate (6.99 g, 35.8 mmol) was added rapidly. The reaction mixture was stirred for an additional 10 minutes and then warmed to room temperature for 4 hours. The crude mixture was taken in EtOAc and washed with water and brine. The aqueous layer was extracted one more time with EtOAc. The combined organic layers were dried over Na2SO4, filtered, concentrated and purified by flash chromatography on a silica gel column (hex:ethyl acetate, 2:1) to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012071B2
Source datasetuspto-grants-2006_03
ORD IDord-73e4db544d084e97b31806d253392fcf
Source noteuspto-grants-2006_03