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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847188Generated: October 31, 2026

Cyanogen Bromide → HCID 12614474, compound

https://huagongshe.com/reaction/847188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 12614416HCID 12614416—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 12614474HCID 12614474—

Reaction Steps

To a stirring solution of 0.36 g of cyanogen bromide, 2.28 g of potassium carbonate in 10 ml of chloroform is added dropwise a solution of 1.0 g of 10-[β-(dimethylamino)ethylthio]dibenz[b,f]oxepin, Example 8, in chloroform. After total addition the reaction mixture is refluxed for 2 hours and the solvent removed leaving an oil. The oil is dissolved in 10 ml of methanol and the methanolic solution refluxed for 10 minutes and again concentrated to recover the oil. The oil is chromatographed through a silica gel column with an eluant of ether. The top fraction is collected and concentrated leaving a white solid, mp 106°-107° C. of 10-[β-(bromo)ethylthio]dibenz[b,f]oxepin.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05140027
Source datasetuspto-grants-1992_08
ORD IDord-f2f3745e63ec4d31a5d3348f850eeb3b
Source noteuspto-grants-1992_08