HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430891Generated: October 31, 2026
p-Bromochlorobenzene → HCID 12327010, compound
https://huagongshe.com/reaction/430891
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Bromochlorobenzene | HCID 7806 | — |
| Reactant | Benzophenone imine | HCID 136809 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis[2-(diphenylphosphino)phenyl] ether | HCID 4285986 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 12327010 | HCID 12327010 | 76% |
Reaction Steps
An oven-dried test tube was charged with tris(dibenzylideneacetone)dipalladium (4.6 mg, 0.005 mmol), bis(2-(diphenylphosphino)phenyl)ether [DPE-phos] (8.2 mg, 0.015 mmol) and 4-bromochlorobenzene (191 mg, 1.0 mmol), capped with a rubber septum, evacuated, and refilled with argon. Benzophenone imine (190 mg, 1.05 mmol) and toluene (2 mL) were added via syringe. The resulting solution was stirred at rt for 5 minutes. The tube was opened and sodium tert-butoxide (135 mg, 1.4 mmol) was added. The tube was again capped with the septum, and additional toluene (2 mL) was added via syringe to wash the solid from the test tube wall into the solution. The solution was stirred at room temperature with a gentle argon purge for 5 minutes, then heated at 80° C. for 1 hour and 30 minutes. The reaction mixture was cooled to room temperature, washed with saturated aqueous sodium chloride (2 mL), and the organic layer was concentrated in vacuo. The product was isolated as a yellow solid (221 mg, 76%) by flash chromatography on silica gel using 5% ethyl acetate in hexanes as eluent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06323366B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-22bc5312351b438f9c68e516fa00c9ad |
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| Source note | uspto-grants-2001_11 |
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