Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79803Generated: October 26, 2026

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

https://huagongshe.com/reaction/79803

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 numberUS08841278B2
Source datasetuspto-grants-2014_09
ORD IDord-ab95781ef51b4af3853a3f3c63b3b1a9
Source noteuspto-grants-2014_09