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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258623Generated: October 31, 2026

4-Aminobiphenyl → HCID 24995122, compound

https://huagongshe.com/reaction/1258623

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminobiphenylHCID 7102—
Reactant3,4-Dimethoxybenzenesulfonyl chlorideHCID 2734183—
SolventPyridineHCID 1049—
ProductHCID 24995122HCID 2499512272.3%

Reaction Steps

To a solution of biphenyl-4-amine (338 mg, 2 mmol) in 10 mL of dry pyridine followed by 529 mg of 3,4-dimethoxybenzenesulfonyl chloride. The solution was stirred at room temperature under Argon. After 21 h, the pyridine was removed in vacuo and flashed off with toluene. The residue was partitioned between EtOAc and 1M NaOH. The organic phase was washed with 1M NaOH until no turbidity was observed on rectification of a small sample. The alkaline phase was made acidic (˜pH 3) with 1M HCl and extracted with EtOAc. After drying over Na2SO4, solvent was removed in vacuo. The crude product (0.79 g) was obtained as a glass which slowly crystallized. Addition of hexane caused complete solidification. The solid was taken up in EtOAc (11 mL), diluted with hexane (11 mL) and seeded to give 534 mg of white needles. The product had mp 171-173° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466182B2
Source datasetuspto-grants-2013_06
ORD IDord-261d9090324643e79f7ff814ecbb266f
Source noteuspto-grants-2013_06