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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508245Generated: October 29, 2026

Sodium hydride → 1,3-Bis(3,6-dibromo-9H-carbazol-9-yl)propan-2-ol

https://huagongshe.com/reaction/508245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant3,6-DibromocarbazoleHCID 274874—
Reactant3,6-dibromo-9-((oxiran-2-yl)methyl)-9H-carbazoleHCID 2775473—
SolventDimethylformamideHCID 6228—
Product1,3-Bis(3,6-dibromo-9H-carbazol-9-yl)propan-2-olHCID 4685104634%

Reaction Conditions

Temperature0 °C

Reaction Steps

3,6-Dibromocarbazole (0.050 g, 0.154 mmol) was dissolved in DMF (1.5 mL) and cooled to 0° C. NaH (60% dispersion in mineral oil, 0.007 g, 0.169 mmol) was added and the reaction was stirred for 45 min at 0° C. 3,6-Dibromo-9-(oxiran-2-ylmethyl)-9H-carbazole (0.059 g, 0.154 mmol) was added and the reaction was stirred at ambient temperature for 24 h. Upon consumption of the starting material by TLC, the reaction was partitioned between EtOAc and H2O. The aqueous layer was washed 3× with EtOAc, and the combined organics were washed with saturated aqueous NaCl, dried over Na2SO4, filtered, and concentrated in vacuo. The crude residue was purified by chromatography (SiO2, 0-50% EtOAc/Hexane) to afford the desired product (37 mg, 34%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09095571B2
Source datasetuspto-grants-2015_08
ORD IDord-920963bc47764eaab496aa36b150340a
Source noteuspto-grants-2015_08