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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417553Generated: October 25, 2026

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

https://huagongshe.com/reaction/417553

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 numberUS08088368B2
Source datasetuspto-grants-2012_01
ORD IDord-ea6af033290545229cea7b2145004052
Source noteuspto-grants-2012_01