HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984630Generated: October 25, 2026
(1,1'-Biphenyl)-2-ol → 6-Phenylhexan-1-amine
https://huagongshe.com/reaction/984630
Participants
| Role | Name | HCID | Charge |
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| Reactant | (1,1'-Biphenyl)-2-ol | HCID 7017 | — |
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | Hexylamine | HCID 8102 | — |
| Reactant | Dodecane | HCID 8182 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 6-Phenylhexan-1-amine | HCID 145558 | — |
Reaction Steps
Copper (I) iodide (10 mg, 0.05 mmol, 5 mol %), anhydrous fine powder potassium phosphate (425 mg, 2.0 mmol) and 2-phenylphenol (34 mg, 0.2 mmol, 20 mol %) were put into a screw-capped test tube with a Teflon septum. Anhydrous toluene (1.0 mL), bromobenzene (105 μL, 1.0 mmol) and n-hexylamine (158 μL, 1.2 mmol) were added by micro-syringe at room temperature under air atmosphere. The reaction mixture was heated at 100° C. for 22 hours. The reaction mixture was then allowed to reach room temperature. Diethyl ether (2 mL), water (2 mL) and dodecane (internal standard, 227 μL) were added. The organic layer was analyzed by GC to give 33% GC yield of N-phenylhexylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06867298B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-5ceefe466195443c91d935e20ef7fdf3 |
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| Source note | uspto-grants-2005_03 |
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