HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362257Generated: October 27, 2026
tert-Butyl methyl ether → 5-Amino-2,3-dihydro-isoindol-1-one
https://huagongshe.com/reaction/2362257
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 5-nitro-2,3-dihydro-1H-isoindol-1-one | HCID 14005625 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | 5-Amino-2,3-dihydro-isoindol-1-one | HCID 21956239 | 48.2% |
Reaction Steps
To a suspension of Fe (1.1 g, 19.6 mmole), NH4Cl (1.5 g, 28 mmole) in a mixture of ethanol/water (30 ml/7 ml) at 80° C. was added a mixture of 5-Nitro-2,3-dihydro-isoindol-1-one (1 g, 5.6 mmole) in 10 ml ethanol. The reaction mixture was stirred at 80° C. for 2 hours. Mixture was cooled down, filtered off, solid was washed with 50 ml ethanol. The filtrate was concentrated, taken into 50 ml ethylacetate, washed with 20 ml water. Organic layer was dried over Na2SO4, filtered and concentrated to give about 900 mg crude. Trituration with methyl t-butylether gave 400 mg pure product, 48% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691816B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-d4f7a5121852462585b29b488e150869 |
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| Source note | uspto-grants-2014_04 |
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