HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908427Generated: October 28, 2026
Ethanol → 2,3,4,9-tetrahydro-1H-carbazol-6-amine
https://huagongshe.com/reaction/1908427
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | 6-nitro-2,3,4,9-tetrahydro-1H-carbazole | HCID 258747 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | 2,3,4,9-tetrahydro-1H-carbazol-6-amine | HCID 14118 | 95.3% |
Reaction Steps
6-Nitro-2,3,4,9-tetrahydro-1H-carbazole (0.100 g, 0.462 mmol) was dissolved in a 40 mL scintillation vial containing a magnetic stir bar and 2 mL of ethanol. Tin (II) chloride dihydrate (1.04 g, 4.62 mmol) was added to the reaction mixture and the resulting suspension was heated at 70° C. for 16 h. The crude reaction mixture was then diluted with 15 mL of a saturated aqueous solution of sodium bicarbonate and extracted three times with an equivalent volume of ethyl acetate. The ethyl acetate extracts were combined, dried over sodium sulfate, and evaporated to dryness to yield 2,3,4,9-tetrahydro-1H-carbazol-6-amine (82 mg, 95%) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598181B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-65900d086f7d4b44afb5bc32c929a45e |
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| Source note | uspto-grants-2013_12 |
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