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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885733Generated: November 1, 2026

Chloroform → HCID 54212508, compound

https://huagongshe.com/reaction/1885733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantCyanogen BromideHCID 10476—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 54133654HCID 54133654—
SolventSodium BicarbonateHCID 516892—
ProductHCID 54212508HCID 5421250895%

Reaction Steps

To a stirred solution of 6.81 g of cyanogen bromide, 4.7 ml of diisopropylethylamine, and 142 ml of chloroform was added, at room temperature with stirring, a solution of 13.7 g of 1,2,3,4,5,6-hexahydro-3,6,12-trimethyl-2,6-methano-9H-pyrrolo[3,2-h][3]benzazocine and 414 ml of chloroform. The mixture was heated at reflux for 2.6 hr, cooled to room temperature, diluted with aqueous sodium bicarbonate solution, and the layers were separated. The organic layer was washed with sodium bicarbonate solution. The combined aqueous layers were extracted with ether. The combined organic layers were washed with brine, dried over anhydrous potassium carbonate, and filtered. Concentration of the filtrate followed by purification by flash chromatography (silica gel, 2% triethylamine/ethyl acetate) afforded 13.5 g (95%) of 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 numberUS05145965
Source datasetuspto-grants-1992_09
ORD IDord-29a7316a4a4e4e1bb7a0a0b8eb8ee7c5
Source noteuspto-grants-1992_09