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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047387Generated: November 1, 2026

Cesium carbonate → Tert-butyl({1-[4-(trifluoromethyl)phenyl]piperidin-4-yl}methyl)carbamate

https://huagongshe.com/reaction/1047387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantBenzene, 1-bromo-4-(trifluoromethyl)-HCID 67872—
ReactantBinap, (A+-)-HCID 634876—
ReactantTert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductTert-butyl({1-[4-(trifluoromethyl)phenyl]piperidin-4-yl}methyl)carbamateHCID 6685325461.8%

Reaction Conditions

Temperature110 °C

Reaction Steps

A solution of 1-bromo-4-trifluoromethyl-benzene (50.0 g; 220 mmol) and piperidin-4-ylmethyl-carbamic acid tert-butyl ester (48.1 g; 220 mmol) in dioxane (1 L) was added to a suspension of palladium (II) acetate (7.41 g; 33 mmol), cesium carbonate (144.8 g; 440 mmol), and 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (31.8 g; 45 mmol) in dioxane (1 L). The resulting mixture was heated to 110° C., and then maintained at that temperature for 28 hr with stirring. The mixture was then allowed to cool to room temperature. Afterward, the reaction mixture was treated with water (2 L) and extracted with dichloromethane (2×1 L). The combined organic phases were dried over sodium sulfate and filtered, and then the solvents were removed under reduced pressure. The resulting residue was dissolved in acetonitrile (1.5 L). Water (1.5 L) was then added with stirring. This resulting in a precipitate, which was filtered and then dried overnight at 40° C. at a pressure of 3 mbar to afford the desired product (48.9 g; 136 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569495B2
Source datasetuspto-grants-2013_10
ORD IDord-5b410fe0dc6541578101b8c64bdb4448
Source noteuspto-grants-2013_10