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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174544Generated: October 30, 2026

1-Bromo-4-iodobenzene → HCID 68485438, compound

https://huagongshe.com/reaction/2174544

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-iodobenzeneHCID 11522—
Reactant3-HydroxypiperidineHCID 23293—
ReactantPotassium Phosphate, TribasicHCID 62657—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethylformamideHCID 6228—
ProductHCID 68485438HCID 68485438—

Reaction Steps

A solution of 1-bromo-4-iodobenzene (Aldrich, 4 g, 14.14 mmol), piperidin-3-ol (Aldrich, 1.14 g, 11.31 mmol), copper (I) iodide (0.269 g, 1.41 mmol) and K3PO4 (6.00 g, 28.3 mmol) in N,N-dimethylformamide (50 mL) under N2 were stirred at 100° C. for 48 h. The reaction mixture was poured into ice and extracted with ethyl acetate. The organic layer was washed successively with water and brine then dried over anhydrous Na2SO4, filtered through celite and concentrated under reduced pressure. The sample was purified on silica gel column chromatography using a cyclohexane to cyclohexane/ethyl acetate 70:30 as eluant. The appropriate fractions were combined and concentrated in vacuo and the residue was triturated with pentane. The resulting solid was filtered, washed with pentane and dried to give the title compound 1-(4-bromophenyl) piperidin-3-ol as a beige powder. LCMS: (M+H)+=256-258; Rt=2.90 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09061998B2
Source datasetuspto-grants-2015_06
ORD IDord-1e71582b0a5d4402bd53bc2811553dd6
Source noteuspto-grants-2015_06