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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904307Generated: October 31, 2026

Cyanogen Bromide → HCID 12614474, compound

https://huagongshe.com/reaction/1904307

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 numberUS04837227
Source datasetuspto-grants-1989_06
ORD IDord-08299c55f0cb45d2b29d33fee5a63933
Source noteuspto-grants-1989_06