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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888365Generated: October 30, 2026

Tert-butyl 3-bromo-5-(2,2,2-trifluoro-1-hydroxyethyl)benzoate → Tert-butyl 3-(5-methylpyridin-2-yl)-5-(2,2,2-trifluoro-1-hydroxyethyl)benzoate

https://huagongshe.com/reaction/888365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 3-bromo-5-(2,2,2-trifluoro-1-hydroxyethyl)benzoateHCID 59539580—
ReactantHCID 178427808HCID 178427808—
CatalystHCID 178418851HCID 178418851—
Solvent1,4-DioxaneHCID 31275—
ProductTert-butyl 3-(5-methylpyridin-2-yl)-5-(2,2,2-trifluoro-1-hydroxyethyl)benzoateHCID 68500334—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of tert-butyl 3-bromo-5-(2,2,2-trifluoro-1-hydroxyethyl)benzoate (5.0 g, 14.1 mmol) and bis(tri-tert-butylphosphine)palladium(0) (0.22 g, 0.42 mmol) in dioxane (70 mL) was added 5-methyl-2-pyridylzinc bromide (0.5 M in THF; 56.3 mL, 28.2 mmol). The reaction mixture was heated to 70° C. After 1 h, additional 5-methyl-2-pyridylzinc bromide (0.5 M in THF; 10 mL, 5.0 mmol) and bis(tri-tert-butylphosphine)palladium(0) (40 mg, 0.078 mmol) were added. After 30 min, the reaction was concentrated. Saturated aqueous sodium potassium tartrate tetrahydrate and saturated aqueous sodium bicarbonate were added. The mixture was extracted with ethyl acetate (3×). The combined organic extracts were washed with brine, dried over sodium sulfate, filtered and concentrated. Purification by silica gel chromatography (100% hexanes→70% hexanes/ethyl acetate) gave the title compound. MS 368.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247401B2
Source datasetuspto-grants-2012_08
ORD IDord-84c672b5097f4cbe81c742a78935b181
Source noteuspto-grants-2012_08