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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217287Generated: October 27, 2026

Dichloromethane → 5-Chloro-1,3-dihydrobenzo[de]isochromene-6-carbonitrile

https://huagongshe.com/reaction/217287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTert-Butyl nitriteHCID 10906—
Reactant5-Amino-1,3-dihydrobenzo[de]isochromene-6-carbonitrileHCID 57898751—
CatalystCupric ChlorideHCID 24014—
SolventAcetonitrileHCID 6342—
Product5-Chloro-1,3-dihydrobenzo[de]isochromene-6-carbonitrileHCID 57898749—

Reaction Conditions

Temperature65 °C

Reaction Steps

tert-Butyl nitrite (27.5 ml, 208 mmol) was added to a suspension of copper (II) chloride (22.5 g, 167 mmol) in anhydrous acetonitrile (500 mL) at room temperature under nitrogen atmosphere. The resulting dark green suspension was heated to the internal temperature of 65° C., and a solution of 5-amino-6-cyano-1H,3H benzo[de]isochromene (29.2 g, 139 mmol) in anhydrous acetonitrile (1000 mL) was added thereto. The reaction solution was stirred at 65° C. for 30 minutes, and then allowed to return to room temperature. The reaction solution was diluted with methylene chloride. The mixture was washed in succession with 1N aqueous hydrochloric acid solution and brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The resulting crude product was purified by silica gel column chromatography using methylene chloride, and dried under reduced pressure. The title compound was obtained as yellow solid material (27.7 g, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193351B2
Source datasetuspto-grants-2012_06
ORD IDord-76146e7c3adf4bb29e8233f7bd4ea205
Source noteuspto-grants-2012_06