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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217286Generated: October 30, 2026

Hydrochloric Acid → 5-Amino-1,3-dihydrobenzo[de]isochromene-6-carbonitrile

https://huagongshe.com/reaction/217286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantChlorotinHCID 6333999—
Reactant5-Nitro-1,3-dihydrobenzo[de]isochromene-6-carbonitrileHCID 57898666—
SolventDiglymeHCID 8150—
Product5-Amino-1,3-dihydrobenzo[de]isochromene-6-carbonitrileHCID 57898751—

Reaction Conditions

Temperature5 °C

Reaction Steps

5-Nitro-6-cyano-1H,3H benzo[de]isochromene (14.3 g, 59.5 mmol) was dissolved in diglyme (297 mL). The reaction vessel was cooled in an ice bath, and a mixed solution of tin (I) chloride (45.1 g, 238 mmol) and concentrated hydrochloric acid (159 mL) was added slowly while the internal temperature was kept below 5° C. The reaction solution was stirred at 5° C. for 2 hours, and then added to a mixture of 50% aqueous sodium hydroxide solution (476 mL) and ice (1400 mL) while stirring vigorously. The precipitate was collected by filtration, and then dissolved in ethyl acetate. The solution was washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resulting crude product was purified by silica gel column chromatography using ethyl acetate, and dried under reduced pressure. The title compound was obtained as pale yellow solid (6.7 g, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193351B2
Source datasetuspto-grants-2012_06
ORD IDord-324a1f762bf342329ccb19ab882bae94
Source noteuspto-grants-2012_06