HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893288Generated: October 29, 2026
1,4-Dibromobenzene → HCID 18507125, compound
https://huagongshe.com/reaction/893288
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dibromobenzene | HCID 7804 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 3-Methoxybenzaldehyde | HCID 11569 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18507125 | HCID 18507125 | 97% |
Reaction Steps
p-Dibromobenzene (7.08 g, 30.0 mmole) was added to 50 ml of anhydrous tetrahydrofuran under nitrogen and the slurry was cooled to -78° C. A solution of n-butyllithium in hexane (1.67 M, 18.0 ml, 30 mmole) was added dropwise over 15 minutes. After stirring for ten minutes at -78° C., 3.8 ml (4.1 g, 30 mmole) of m-anisaldehyde was added dropwise over five minutes. After stirring for 15 minutes, the reaction was quenched with 10 ml of saturated aqueous ammonium chloride solution and was allowed to warm to room temperature. The reaction solution was diluted with 300 ml of diethyl ether and washed with three 50 ml portions of 1.0 M aqueous sodium bisulfite, followed by 50 ml of 1.0 M sodium hydroxide, 100 ml of water, and 100 ml of saturated sodium chloride. After drying over magnesium sulfate, the solvent was removed to give 8.5 g (97%) of crude (4-bromophenyl)(3-methoxyphenyl)-methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05124330 |
|---|
| Source dataset | uspto-grants-1992_06 |
|---|
| ORD ID | ord-2efa4d6e18da4145b6174cf54f60b10f |
|---|
| Source note | uspto-grants-1992_06 |
|---|