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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764107Generated: November 3, 2026

Isoindoline → HCID 70616527, compound

https://huagongshe.com/reaction/1764107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoindolineHCID 422478—
ReactantHCID 53945814HCID 53945814—
SolventEthanolHCID 702—
ProductHCID 70616527HCID 7061652741%

Reaction Steps

The process for the preparation of this compound and its physical properties will be given below. A solution of 3.46 grams of o-chlorocinnamyl chloride and 4.41 grams of isoindoline in 20 milliliters of ethanol is stirred for 12 hours at room temperature. After cmmpletion of the reaction, the solvent is distilled off. The resulting residue is then rendered alkaline by the addition of 10% sodium hydroxide and extracted with chloroform. The chloroform layer is then purified by silica gel column chromatography, and the resulting oily product is treated as in Example 1-a to obtain 2.32 grams (yield 41% of N-(o-chlorocinnamyl)-isoindoline hydrochloride as crystals having a melting point of 170°-172° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04115398
Source datasetuspto-grants-1978_09
ORD IDord-d0199f8c7b8f4fc59e8739c3a35b9268
Source noteuspto-grants-1978_09