HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron Trichloride → HCID 67352771, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron Trichloride | HCID 25135 | — |
| Reactant | HCID 67355479 | HCID 67355479 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67352771 | HCID 67352771 | 103.7% |
Reaction Steps
Ethyl 2-(4-chlorophenyl)-5-isopropoxy-6-nitrobenzofuran-3-carboxylate (11 g, 27.2 mmol) was dissolved in anhydrous DCM (150 mL) and cooled in an ice bath under an atmosphere of nitrogen. Boron trichloride (41 mL, 41.0 mmol) was added over ˜20 minutes. After the reaction was complete, the reaction mixture was quenched by pouring into an ice/water mixture. The mixture was extracted with DCM, and the combined organic layers were dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum to give ethyl 2-(4-chlorophenyl)-5-hydroxy-6-nitrobenzofuran-3-carboxylate (10.2 g, 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09119868B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-87c0dd62715e4569b4f394823a4626f5 |
| Source note | uspto-grants-2015_09 |