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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730069Generated: October 30, 2026

Cyanide → HCID 57833595, compound

https://huagongshe.com/reaction/730069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanideHCID 5975—
ReactantHCID 57833591HCID 57833591—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystPalladiumHCID 23938—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventDimethylformamideHCID 6228—
ProductHCID 57833595HCID 57833595—

Reaction Steps

A solution of trifluoromethanesulfonic acid 9-[8-(2,2, 2-trifluoroacetyl)-8-aza-bicyclo[3.2.1]oct-3-ylidene]-9H-xanthen-4-yl ester in a deoxygenated solvent such as dimethyl formamide (0.5 to 2 M solution) may be treated with a catalytic amount of a palladium catalyst such as tetrakis(triphenylphosphine) palladium ( 0.01 to 0.1 equiv) and a cyanide source such as zinc cyanide (1.5 to 3 equiv). The mixture may be heated to 100° C. to 150° C. under an argon atmosphere for 1 to 5 hr. After cooling, the mixture may be partitioned between a saturated sodium bicarbonate solution and an organic solvent such as ethyl acetate. The organic phase may be separated, dried over an appropriate drying agent such as sodium sulfate, filtered, and evaporated. The residue may be purified over silica gel using a mixture of organic solvents or via reverse phase chromatography to yield Compound 2b.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582650B2
Source datasetuspto-grants-2009_09
ORD IDord-b8fac990b34e4118b4b18deebfbc8184
Source noteuspto-grants-2009_09