HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34381Generated: October 25, 2026
Dichloromethane → 1-(2-Amino-4-methylphenyl)-5-bromoindoline hydrochloride
https://huagongshe.com/reaction/34381
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-(5-Bromo-1-indolinyl)-3-nitrotoluene | HCID 13823341 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(2-Amino-4-methylphenyl)-5-bromoindoline hydrochloride | HCID 13823343 | 39% |
Reaction Steps
To a warm solution of 4-(5-bromo-1-indolinyl)-3-nitrotoluene (10 g, 0.03 mole) in dichloromethane (40 ml) and ethanol (160 ml) was added 1% platinum-on-carbon (2.0 gm). The mixture was shaken under hydrogen (57 psi) for 3.5 hours. The mixture was filtered and concentrated. The residue was dried under vacuum at 55° C. Purification was accomplished by flash chromatography over silica gel (100 g), eluted with a mixture of hexane:dichloromethane (3:1, 2 1 and 1:1, 1 1). The fractions containing pure product were pooled and concentrated. The residue was dissolved in ether (250 ml) and added to a methanol/hydrogen chloride solution, and the mixture was stirred at 0° C. for 10 minutes. The precipitate was filtered and dried to afford 4.0 g (39%) of product, mp 195°-200° C. dec.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04761412 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-8e5f9325c24a4c0aba0463eac1d7676f |
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| Source note | uspto-grants-1988_08 |
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