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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494828Generated: October 30, 2026

2-Benzyl-5-nitroisoindoline → 2-Benzyl-2,3-dihydro-1H-isoindol-5-ylamine

https://huagongshe.com/reaction/1494828

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Benzyl-5-nitroisoindolineHCID 12065977—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2-Benzyl-2,3-dihydro-1H-isoindol-5-ylamineHCID 315924481.6%

Reaction Steps

4.0 g of 2-benzyl-5-nitroisoindoline prepared in Reference Example 2-(2) was dissolved in 40 ml of methanol and 800 mg of 10% palladium on carbon was added to the solution. The catalytic hydrogenation was performed for 32 hours at room temperature and under atmospheric pressure. After removing the catalyst by filtration, the filtrate was concentrated to obtain 2.88 g of 2-benzyl-5-aminoisoindoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05026856
Source datasetuspto-grants-1991_06
ORD IDord-e57fabad950d454c8eee0c892aefd3dc
Source noteuspto-grants-1991_06