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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248117Generated: October 30, 2026

Cyanogen Bromide → HCID 53643109, compound

https://huagongshe.com/reaction/2248117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 53780973HCID 53780973—
SolventChloroformHCID 6212—
ProductHCID 53643109HCID 53643109162.5%

Reaction Steps

To a stirred solution of 1.68 g of cyanogen bromide and 35 ml of chloroform was added, at room temperature with stirring under nitrogen, a solution of 3.8 g of 10-chloro-1,2,3,4,5,6-hexahydro-3,6,12-trimethyl-2,6-methano-9H-pyrrolo[3,2-h][3]-benzazocine and 100 ml of chloroform. The mixture was heated at reflux for 2 hr, under nitrogen, and cooled to room temperature. Dilute aqueous sodium bicarbonate solution was added and the layers separated. The organic layer was extracted with dilute aqueous sodium bicarbonate solution. The combined aqueous layers were extracted with ether and the combined organic layers were washed with brine, dried over anhydrous potassium carbonate and filtered. The filtrate was concentrated and the residue was purified by flash column chromatography (silica gel, 2% triethylamine/ethyl acetate) to afford 6.41 g (78%) of 10-chloro-3-cyano-6,12-dimethyl-1,2,3,4,5,6-hexahydro-2,6-methano-9H-pyrrolo-[3,2-h][3]benzazocine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05037985
Source datasetuspto-grants-1991_08
ORD IDord-319833ff359d4a52bb54b4e84ff8e433
Source noteuspto-grants-1991_08