HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494342Generated: October 29, 2026
Hydrochloric Acid → 4'-Methyl[1,1'-biphenyl]-2-carbaldehyde
https://huagongshe.com/reaction/494342
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Bromotoluene | HCID 7805 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 123334-93-0 | HCID 10775151 | — |
| Product | 4'-Methyl[1,1'-biphenyl]-2-carbaldehyde | HCID 1394009 | 51% |
Reaction Steps
To a suspension of magnesium metal (1.1 g) in THF (3 ml) was added dropwise a solution of 4-bromotoluene (7.5 g) in THF (10 ml) under gentle reflux. The resulting solution of the Grignard reagent was added dropwise to an ice-cooled, stirred solution of N-(2-methoxyphenyl)methylidenecyclohexylamine (4.3 g) in THF (30 ml). The reaction mixture was stirred at room temperature for 1.5 hours, followed by heating under reflux for 7 hours. After addition of ice-water, the reaction mixture was acidified with conc. hydrochloric acid. The reaction mixture was extracted with ethyl acetate and the extract was washed with 1N-hydrochloric acid and water, dried and evaporated to dryness. The residue was purified by column chromatography on silica gel to give pale yellow syrup (2.0 g, 51%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07538133B2 |
|---|
| Source dataset | uspto-grants-2009_05 |
|---|
| ORD ID | ord-4165a6022fef49b29a37d373d991f53f |
|---|
| Source note | uspto-grants-2009_05 |
|---|