HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764111Generated: October 25, 2026
Sodium Hydroxide → N-(m-nitrocinnamyl)-isoindoline hydrochloride
https://huagongshe.com/reaction/1764111
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-(3-Chloro-propenyl)-3-nitro-benzene | HCID 4377749 | — |
| Reactant | 2,3-dihydro-1H-isoindole hydrochloride | HCID 12311031 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(m-nitrocinnamyl)-isoindoline hydrochloride | HCID 70616192 | 52% |
Reaction Steps
The process for the preparation of this compound and its physical properties will be given below. A solution of 5.68 grams of isoindoline hydrochloride and 2.86 grams of sodium hydroxide in 15 milliliters of water is added to a solution of 6.8 grams of m-nitrocinnamyl chloride in 160 milliliters of ethanol, and the mixture is stirred for 10 hours at room temperature. After completion of the reaction, the reaction product is concentrated, and the residue is extracted with chloroform. The extract is then purified by silica gel column chromatography, following which the resulting oily product is converted to a hydrochloride in a customary manner and recrystallized from ethanol to obtain 5.6 grams (yield 52%) of N-(m-nitrocinnamyl)-isoindoline hydrochloride as crystals having a melting point of 208°-210° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04115398 |
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| Source dataset | uspto-grants-1978_09 |
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| ORD ID | ord-0cb01a295cd8484ba4fc4671b7de70c3 |
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| Source note | uspto-grants-1978_09 |
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