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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776211Generated: October 30, 2026

Carbazole → HCID 86702142, compound

https://huagongshe.com/reaction/1776211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbazoleHCID 6854—
ReactantSodium hydrideHCID 24758—
Reactant1-Butyne, 3-chloro-3-methyl-HCID 70679—
SolventDimethylformamideHCID 6228—
ProductHCID 86702142HCID 8670214249%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of carbazole (2.500 g, 15.0 mmol) in anhydrous N,N-dimethylformamide (30 mL) at 0° C. was added 60% sodium hydride in mineral oil (0.718 g, 17.9 mmol) and the mixture was stirred at 0° C. for 1 hr. 3-Chloro-3-methyl-1-butyne (2.300 g, 22.4 mmol) was added and the reaction mixture was stirred at 0° C. for 1 hr and then slowly warmed to room temperature and stirred for 16 hrs. The mixture was partitioned between water and ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, dried (anhydrous sodium sulfate), filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography (10-70% methylene chloride/hexanes) to afford the desired product as a light brown solid (1.7 g, 49%). 1H NMR (300 MHz, CDCl3) δ 8.10 (d, 2H, J=7.5 Hz), 8.04 (d, 2H, J=8.7 Hz), 7.41 (td, 2H, J=8.1, 1.5 Hz), 7.24 (t, 2H, J=7.5 Hz), 2.67 (s, 1H), 2.28 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09265772B2
Source datasetuspto-grants-2016_02
ORD IDord-2f316381517b4febac6a8285a3c415c4
Source noteuspto-grants-2016_02