HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217299Generated: October 25, 2026
Sodium Hydroxide → 1-(5-chloro-1H,3H-benzo[de]isochromen-6-yl)-ethylidene-amine
https://huagongshe.com/reaction/217299
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium potassium tartrate tetrahydrate | HCID 2724148 | — |
| Reactant | Trimethylaluminium toluene | HCID 18425018 | — |
| Reactant | 5-Chloro-1,3-dihydrobenzo[de]isochromene-6-carbonitrile | HCID 57898749 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(5-chloro-1H,3H-benzo[de]isochromen-6-yl)-ethylidene-amine | HCID 57898832 | 102.8% |
Reaction Steps
5-Chloro-1H,3H-benzo[de]isochromen-6-carbonitrile (20 g, 87.08 mmol) obtained in Step 5 of Example 71 was suspended in anhydrous toluene (100 mL) under nitrogen atmosphere, and 2 M trimethyl aluminum-toluene solution (218 mL, 435 mmol) was added at room temperature. The obtained solution was stirred while heating in a 105° C. oil bath for 12 hours. The reaction solution was cooled to room temperature, and then slowly poured into an aqueous solution of potassium sodium (+)-tartarate tetrahydrate (184 g). 2 N aqueous sodium hydroxide solution (250 mL) was additionally added, and after stirring for 30 minutes, this was extracted with ethyl acetate (500 mL). The separated organic layer was washed with water (300 mL) and brine, then dried over anhydrous sodium sulfate, filtered, concentrated, and thus, 1-(5-chloro-1H,3H-benzo[de]isochromen-6-yl)-ethylidene-amine (22 g) was obtained as an orange-colored oil like substance.
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-2385df99f89148f78991290de1d2952a |
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| Source note | uspto-grants-2012_06 |
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