HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880495Generated: October 26, 2026
1,5-Dinitronaphthalene → 1-Naphthalenamine, 5-nitro-
https://huagongshe.com/reaction/880495
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,5-Dinitronaphthalene | HCID 11803 | — |
| Reactant | Sodium Sulfide | HCID 14804 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Naphthalenamine, 5-nitro- | HCID 76759 | 42% |
Reaction Steps
A 70° C. solution of sodium sulfide (3.17 g, 32.97 mmol) and sodium bicarbonate in water (7 mL) was added dropwise to suspension of 1,5-dinitro naphthalene (2.0 g, 9.16 mmol) in methanol (30 mL) at reflux and the resultant mixture was stirred for 5 min. The mixture was cooled to 0° C., quenched with ice and stirred for a further 10 min followed by acidification with concentrated hydrochloric acid. The resulting mixture was stirred for 30 min then washed with ethyl acetate (2×50 mL). The aqueous layer was basified with aqueous ammonia and extracted with ethyl acetate (2×100 mL). The combined organic layers were washed with water (2×50 mL), brine (2×50 mL), dried over anhydrous sodium sulphate, filtrated and concentration in vacuo afforded of 5-nitronaphthalen-1-amine (710 mg, 42%) as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993574B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-85b8a0bf8f34449ba499ffd3e6cadb34 |
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| Source note | uspto-grants-2015_03 |
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