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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424780Generated: November 2, 2026

Boron Trichloride → HCID 67352771, compound

https://huagongshe.com/reaction/1424780

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 numberUS08927593B2
Source datasetuspto-grants-2015_01
ORD IDord-df48225190e14d5ca5b5ad7064f17ef0
Source noteuspto-grants-2015_01