HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28650Generated: October 27, 2026
Hydrochloric Acid → HCID 66571439, compound
https://huagongshe.com/reaction/28650
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 4-Chloro-1-ethyl-2-iodobenzene | HCID 68984613 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66571439 | HCID 66571439 | 52% |
Reaction Steps
To a solution of 4-chloro-1-ethyl-2-iodo-benzene (5 g, 18.8 mmol) in anhydrous tetrahydrofuran (40 ml), cooled to −30° C., was added isopropyl magnesium chloride (2 M in tetrahydrofuran, 10 ml, 20 mmol) dropwise. After stirring at −30° C. for 30 minutes, trimethyl borate (4.2 ml, 38 mmol) was added dropwise and the mixture was stirred for 1.5 hours. The mixture was treated with hydrochloric acid (1 M, 25 ml), ethyl acetate (100 ml), and saturated aqueous sodium chloride solution (100 ml). The organic layer was dried over sodium sulfate and concentrated under reduced pressure. The residue was treated with hexane (50 ml) and the solid was filtered to afford 5-chloro-2-ethyl-phenyl boronic acid (1.8 g, 52% yield) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07419984B2 |
|---|
| Source dataset | uspto-grants-2008_09 |
|---|
| ORD ID | ord-58efa064964f4c97b743fc15c07741f1 |
|---|
| Source note | uspto-grants-2008_09 |
|---|