HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592814Generated: November 1, 2026
3-Aminophenylboronic acid → HCID 68907652, compound
https://huagongshe.com/reaction/1592814
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Aminophenylboronic acid | HCID 92269 | — |
| Reactant | 3-Bromo-2-chlorothiophene | HCID 2724559 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Potassium Carbonate | HCID 11430 | — |
| Product | HCID 68907652 | HCID 68907652 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07294616B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-e64a2308979d4f189d4ef5939e1f651d |
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| Source note | uspto-grants-2007_11 |
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