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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468342Generated: October 29, 2026

Ethanol → 2,3,4,9-tetrahydro-1H-carbazol-6-amine

https://huagongshe.com/reaction/468342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantStannous chloride dihydrateHCID 61436—
Reactant6-nitro-2,3,4,9-tetrahydro-1H-carbazoleHCID 258747—
SolventSodium BicarbonateHCID 516892—
Product2,3,4,9-tetrahydro-1H-carbazol-6-amineHCID 1411895.3%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623905B2
Source datasetuspto-grants-2014_01
ORD IDord-287438f9bba0431eae4d3b4d0f2a860e
Source noteuspto-grants-2014_01