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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592814Generated: November 1, 2026

3-Aminophenylboronic acid → HCID 68907652, compound

https://huagongshe.com/reaction/1592814

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Aminophenylboronic acidHCID 92269—
Reactant3-Bromo-2-chlorothiopheneHCID 2724559—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventPotassium CarbonateHCID 11430—
ProductHCID 68907652HCID 68907652—

Reaction Conditions

Temperature90 °C

Reaction Steps

3-bromo-2-chlorothiophene (1.00 mL), 3-aminophenylboronic acid (2.2266 g) and palladium tetrakistriphenylphosphine (544.8 mg) were combined in a mixture of 40 mL of dimethoxyethane and 15 mL of 2.0 M aqueous potassium carbonate under an atmosphere of dry N2. The reaction mixture was heated at 90° C. overnight. The reaction mixture was then cooled to room temperature and partitioned between EtOAc and water. The EtOAc layer was then dried over MgSO4, filtered and concentrated under vacuum. The resulting residue was purified using silica gel chromatography eluting with a 1:1 solution of DCM/Hexanes, followed by a 4:3 solution of DCM/Hexanes and finally a 2:1 solution of DCM/Hexanes, to give 1.80 g of 3-(2-chlorothiophen-3-yl)benzenamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07294616B2
Source datasetuspto-grants-2007_11
ORD IDord-e64a2308979d4f189d4ef5939e1f651d
Source noteuspto-grants-2007_11