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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877854Generated: November 2, 2026

Cyanogen Bromide → HCID 87298019, compound

https://huagongshe.com/reaction/877854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantN-Ethyl-2,6-dimethylanilineHCID 12539332—
SolventTolueneHCID 1140—
ProductHCID 87298019HCID 87298019—

Reaction Steps

N-ethyl-2,6-dimethylaniline (5.9 g, 39.6 mmol) was added to a stirred solution of cyanogen bromide (2.1 g, 19.8 mmol) in toluene (50 mL). The reaction mixture was allowed to react overnight at room temperature during which a solid formed. A small temperature rise to 30° C. was observed. The suspension was filtered and the residue was washed with toluene (3×25 mL). The combined filtrates were evaporated to dryness by rotatory evaporation and the resulting residue was purified by Kugelrohr distillation (0.2 mbar, 110-125° C.) yielding a brown oil. Yield: 3.09 g (90%). The residue (N-ethyl-2,6-dimethylaniline hydrobromide) of the filtration step was used in the following synthetic step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987393B2
Source datasetuspto-grants-2015_03
ORD IDord-31b0cc3ef0124165a4394cea155ab67f
Source noteuspto-grants-2015_03