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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879536Generated: October 26, 2026

Hydrochloric Acid → 7-(benzyloxy)-9H-carbazol-2-amine

https://huagongshe.com/reaction/1879536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactanttert-butyl 7-(benzyloxy)-9H-carbazol-2-ylcarbamateHCID 66933893—
Solvent1,4-DioxaneHCID 31275—
Product7-(benzyloxy)-9H-carbazol-2-amineHCID 59282948102%

Reaction Steps

To tert-butyl 7-(benzyloxy)-9H-carbazol-2-ylcarbamate (200 mg, 0.51 mmol) was added 10 mL of a 4 M HCl in dioxane solution. The mixture was stirred at rt for 4 h and concentrated under reduced pressure. The residue was washed with ether (15 mL) and suspended in EtOAc (50 mL). To this suspension was added 10 mL of a NaHCO3 (sat.) and the mixture was stirred for 5 min. The organic layer was dried over MgSO4 and concentrated to afford 7-(benzyloxy)-9H-carbazol-2-amine as a brown solid (150 mg, 100%). 1H NMR (400 MHz, DMSO-d6) δ 11.33 (s, 1H), 7.99 (d, J=8.4 Hz, 1H), 7.92 (d, J=8.8 Hz, 1H), 7.42 (d, J=6.8 Hz, 2H), 7.34-7.21 (m, 3H), 7.27-7.23 (m, 1H), 7.00-6.97 (m, 2H), 6.81 (dd, J=8.8, 2.4 Hz, 1 H), 5.12 (s, 2H); MS (ESI) m/z 289 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318132B2
Source datasetuspto-grants-2012_11
ORD IDord-45c06af874964df794eeb8f4abc0a097
Source noteuspto-grants-2012_11