HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992192Generated: October 29, 2026
Hydrochloric Acid → HCID 178447829, compound
https://huagongshe.com/reaction/992192
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | 5,6-Difluoro-2-bromonaphthalene | HCID 11413832 | — |
| Reactant | HCID 178447892 | HCID 178447892 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178447829 | HCID 178447829 | — |
Reaction Steps
To a THF solution of an organic lithium reagent prepared from 5,6-difluoro-2-bromonaphthalene were added dropwise 4-iodo-1-(trans-4-propylcyclohexyl)benzene and a THF solution of tetrakis(triphenylphosphine)palladium (0) in the catalytic amount. The reaction mixture were then stirred at room temperature for 3 hours. To the reaction mixture were then added water and toluene to terminate the reaction. To the reaction solution was then added diluted hydrochloric acid until the aqueous phase became weakly acidic. The reaction solution was then extracted with toluene. The material thus extracted and the organic phase were together washed with water and then with saturated brine, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain an oily matter. The oily matter was purified through silica gel column chromatography (hexane), and then recrystallized from ethanol to obtain 5,6-difluoro-2-[4-(trans-4-propylcyclohexyl)phenyl]naphthalene in the form of white crystal,
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06468607B1 |
|---|
| Source dataset | uspto-grants-2002_10 |
|---|
| ORD ID | ord-25e8d30bdf144ba4adb54a9fa51a0a68 |
|---|
| Source note | uspto-grants-2002_10 |
|---|