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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371018Generated: October 26, 2026

Tert-butyl 2-[4-(bromomethyl)phenoxy]-2,2-difluoroacetate → Methyl 4-[1-{4-[2-(tert-butoxy)-1,1-difluoro-2-oxoethoxy]benzyl}-2-(4-fluorophenyl)-2-oxoethyl]benzoate

https://huagongshe.com/reaction/1371018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 2-[4-(bromomethyl)phenoxy]-2,2-difluoroacetateHCID 15391315—
ReactantMethyl 4-[2-(4-fluorophenyl)-2-oxoethyl]benzoateHCID 18510220—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-[1-{4-[2-(tert-butoxy)-1,1-difluoro-2-oxoethoxy]benzyl}-2-(4-fluorophenyl)-2-oxoethyl]benzoateHCID 1851024160.4%

Reaction Steps

To a solution of methyl-4-[2-(4-fluorophenyl)-2-oxoethyl]benzoate (0.150 g, 0.551 mmol) (Example 1, Step 2) in degassed THF at −20° C. was added potassium tert-butoxide (0.606 ml), followed by a solution of tert-butyl 2-[4-(bromomethyl)phenoxy]-2,2-difluoroacetate (H. Fretz, Tetrahedron 54, 4849, 1998) (0.203 g, 0.604 mmol) in THF (0.5 ml). The reaction was allowed to warm slowly to room temperature, and was then quenched with saturated ammonium acetate solution and extracted with ethyl acetate. The organic phase was dried over sodium sulfate, filtered and evaporated to dryness. The residue was purified by flash chromatography using toluene/ethyl acetate 5% giving 0.176 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583126B2
Source datasetuspto-grants-2003_06
ORD IDord-88b879f0a0234b94b02516e1f9d2a99b
Source noteuspto-grants-2003_06