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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1847741Generated: October 29, 2026

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

https://huagongshe.com/reaction/1847741

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 numberUS08952049B2
Source datasetuspto-grants-2015_02
ORD IDord-d9b9d2ace9f0467bb1202e16445d4954
Source noteuspto-grants-2015_02