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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576269Generated: November 3, 2026

Cyanogen Bromide → HCID 86733956, compound

https://huagongshe.com/reaction/1576269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantHCID 86733957HCID 86733957—
SolventDichloromethaneHCID 6344—
ProductHCID 86733956HCID 86733956—

Reaction Steps

4-Methoxy-1'-methyl-9,10-dihydroanthracene-9-spiro-4'-piperidine (12.6 g.) and cyanogen bromide (5.6 g.) in methylene chloride (250 ml.) are stirred at room temperature for 18 hours. The reaction mixture is evaporated to dryness, and the residue is taken up in chloroform, the solution washed with water and with brine, dried (MgSO4), and evaporated to give a brown oil which is chromatographed rapidly on silica gel. Elution with ethyl acetate affords pure 1'-cyano-4-methoxy-9,10-dihydroanthracene-9-spiro-4'-piperidine as an oil, characterised by the peak at 2200 cm-1 (C≡N stretching) in its infra-red spectrum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03979513
Source datasetuspto-grants-1976_09
ORD IDord-408bcd9293a546f9878f02442e9eba1f
Source noteuspto-grants-1976_09