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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | 5-Amino-1,3-dihydrobenzo[de]isochromene-6-carbonitrile | HCID 57898751 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-Chloro-1,3-dihydrobenzo[de]isochromene-6-carbonitrile | HCID 57898749 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193351B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-76146e7c3adf4bb29e8233f7bd4ea205 |
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| Source note | uspto-grants-2012_06 |
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