Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 71853Generated: October 26, 2026

1,4-Dibromobenzene → 4-Bromo-4'-t-butoxycarbonylaminobiphenyl

https://huagongshe.com/reaction/71853

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobenzeneHCID 7804—
ReactantPotassium CarbonateHCID 11430—
Reactant(4-Boc-Aminophenyl)Boronic AcidHCID 3613184—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
Product4-Bromo-4'-t-butoxycarbonylaminobiphenylHCID 5961053459%

Reaction Conditions

Temperature80 °C

Reaction Steps

4-tert-Butoxycarbonylamino-phenylboronic acid (500 mg, 2.11 mmol), 1,4-dibromo-benzene (2.00 g, 8.44 mmol) Pd(PPh3)4 (122 mg, 0.106 mmol) and a 2 M aqueous solution of potassium carbonate (4.2 mL, 8.44 mmol) were degassed in 1,2-dimethoxyethane (20 mL) for 10 min. The stirred suspension was heated to 80° C. for 3 hours then diluted with ethyl acetate (60 mL) and washed with water and brine. The organic phase was dried over magnesium sulfate and concentrated. The residue was purified by silica column chromatography (0% to 20% EtOAc/hexanes) to provide (4′-Bromo-biphenyl-4-yl)-carbamic acid tert-butyl ester (430 mg, 59%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822430B2
Source datasetuspto-grants-2014_09
ORD IDord-975ad5d4f0f04d9bbea677d976312ba1
Source noteuspto-grants-2014_09