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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272277Generated: October 31, 2026

Boron Trichloride → HCID 67352771, compound

https://huagongshe.com/reaction/2272277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron TrichlorideHCID 25135—
ReactantHCID 67355479HCID 67355479—
SolventDichloromethaneHCID 6344—
ProductHCID 67352771HCID 67352771103.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09119868B2
Source datasetuspto-grants-2015_09
ORD IDord-87c0dd62715e4569b4f394823a4626f5
Source noteuspto-grants-2015_09