HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1588934Generated: November 2, 2026
5-Bromo-1,2,3-trimethoxybenzene → HCID 19754891, compound
https://huagongshe.com/reaction/1588934
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Bromo-1,2,3-trimethoxybenzene | HCID 75885 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | HCID 54075683 | HCID 54075683 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19754891 | HCID 19754891 | — |
Reaction Steps
To a stirred, cold (-15° C.) solution Of 3,4,5-trimethoxybromobenzene (965 mg, 3.9 mmol) in ethyl ether (15 ml) is added n-BuLi (3 ml of 1.6 M solution in hexane). The reaction mixture is stirred at -8° C. for 10 min., diluted with THF (5 ml) and warmed to 0° C. After stirring for 5 min., the reaction is cooled to -30° C. and a solution of 4-formyl-3-methylbenzoic acid N-isopropyl-N-cyclohexyl amide (1.12 g, 3.9 mmol) in THF (5 ml) is added. After stirring at -30° C. for 10 min. and warming to room temperature, the reaction is poured onto 0.5 N KHSO4 and extracted with ethyl acetate. The organic layer is washed with saturated NaCl solution and dried (MgSO4). The drying agent is filtered and the filtrate concentrated in vacuo to give the crude product. This is chromatographed on silica gel using mixtures of ethyl acetate and hexane as eluents to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05223539 |
|---|
| Source dataset | uspto-grants-1993_06 |
|---|
| ORD ID | ord-eaec4d1e607143e0890a8827afa9096d |
|---|
| Source note | uspto-grants-1993_06 |
|---|